Synthetic techniques and intermediates for polyhydroxy, dienyl lactone derivatives

ABSTRACT

Synthetic methods for lactone-containing compounds such as the discodermolides are provided, as are compounds which mimic the chemical and/or biological activity thereof, and methods and intermediates useful in their preparation.

GOVERNMENT SUPPORT

Certain of the inventors were supported by National Institutes of Health Grant GM-29028.

CROSS-REFERENCED RELATED APPLICATION

This Application is a continuation-in-part of U.S. patent application Ser. No. 08/759,817, filed Dec. 3, 1996 now U.S. Pat. No. 5,789,605.

FIELD OF THE INVENTION

This invention relates to lactone-containing compounds such as discodermolide, to compounds which mimic the chemical and/or biological activity thereof, and to methods and intermediates useful in their preparation.

BACKGROUND OF THE INVENTION

In 1990, Gunasekera and co-workers at the Harbor Branch Oceanographic Institute reported the isolation of (+)-discodermolide (1), an architecturally novel metabolite of the marine sponge Discodermia dissoluta (0.002% w/w). (See, Gunasekera, et al., J. Org. Chem. 1990, 55, 4912. Correction: J. Org. Chem. 1991, 56, 1346). ##STR1##

Initial studies revealed that (+)-discodermolide suppresses both the two-way mixed-lymphocyte reaction and the concanavalin A-induced mitogenesis of murine splenocytes in vitro with no associated cytotoxicity. Moreover, (+)-1 suppresses the in vivo graft-vs.-host splenomegaly response induced by injection of parental splenocytes into F1 recipient mice, with potency intermediate between those of cyclosporin A and FK506. (Longley, et al., Transplantation 1991, 52, 650; Longley, et al., Transplantation 1991, 52, 656; Longley, et al. Ann. N.Y. Acad. Sci. 1993, 696, 94). These findings stimulated the recent discovery that (+)-1 arrests cell development at the M phase by binding and stabilizing mitotic spindle microtubules; thus discodermolide resembles taxol in its mode of action, but the microtubule binding affinity of 1 is much higher. (ter Haar, et al., Biochemistry 1996, 35, 243; Hung, et al., Chemi. & Biol. 1996, 3, 287). These and other results suggest that (+)-discodermolide holds considerable promise as an anticancer agent. The scarcity of natural material however has precluded a complete evaluation of its biological profile.

The absolute configuration of discodermolide remained undefined until Schreiber et al. synthesized both antipodes of 1. (Nerenberg, et al. J. Am. Chem. Soc. 1993, 115, 12621; Hung, et al., Chem. & Biol. 1994, 1, 67). Interestingly, the unnatural (-) antipode also displays significant immunosuppressant activity.

There is, therefore, a need for improved synthetic methods for the preparation of polyhydroxy, dienyl lactones such as the discodermolides, as well as a need for compounds having similar chemical and/or biological activity.

OBJECTS OF THE INVENTION

It is one object of the present invention to provide polyhydroxy, dienyl lactones and mimics thereof.

It is a further object to provide processes for the preparation of such compounds and their mimics.

It is another object of this invention to provide intermediates useful in such processes.

SUMMARY OF THE INVENTION

These and other objects are satisfied by the present invention, which, in one aspect, provides synthetic methods for the discodermolides and other polyhydroxylactones. In preferred embodiments, such methods involve contacting a phosphonium salt of formula I: ##STR2## with base and an alkylthiol of formula II: ##STR3## to form a diene of formula III: ##STR4## wherein: R₁, R₂, R₃, R₇, R₈, R₁₁, R₁₂ and R₁₃ are, independently, C₁ -C₁₀ alkyl;

R₆ is H or C₁ -C₁₀ alkyl;

X is a halogen;

Z, Z₁, and Z₂ are, independently, O, S or NR';

R₄, R₉, R₁₄, and R₁₅ are, independently, acid labile hydroxyl protecting groups;

R₅ is C₆ -C₁₄ aryl;

Y is O, S or NR';

R' and R₁₆ are, independently, hydrogen or C₁ -C₆ alkyl; and

R₁₈ is C₆ -C₁₄ aryl.

In another embodiment, compounds of formula I are contacted with compounds of the following formula XXIII: ##STR5## to form a diene of formula XXXXX: ##STR6##

In another aspect, the methods of the invention involve producing an alkene of formula IV. ##STR7## This can be accomplished by contacting an organometallic reagent of formula Va: ##STR8## with a vinyl halide of formula VIa: ##STR9## wherein M is Li, Cu, Mg, or Zn and R₁₀ is an acid stable hydroxyl protecting group and all other variables are as defined above. Alternatively, a vinyl halide of formula Vb: ##STR10## can be contacted with an organometallic compound of formula VIb: ##STR11##

In yet another aspect, the methods of the invention involve compounds having formula VII. ##STR12## by contacting a diene of formula VIIIa: ##STR13## with an organometallic compound having formula Va wherein R₂₄ is hydrogen and R₂₅ is hydrogen or an acid stable hydroxyl protecting group. Alternatively, an organometallic compound having formula VIIIb can be contacted with a vinyl halide having formula Vb. ##STR14##

The methods of the invention also involve producing dienes having formula VIIIa by contacting phosphonium salts having formula IX: ##STR15## with base and alkylthiol compounds having formula II.

The present invention also provides synthetic intermediates which are useful in the preparation of polyhydroxylactones, including the compounds having formulas I-IX and X: ##STR16## wherein: R₁₉, R₂₀, R₂₁ and R₂₂ are, independently, C₁ -C₁₀ alkyl; and

R₂₃ is C₇ -C₁₅ aralkyl.

The present invention also provides compounds which mimic the chemical and/or biological activity of the discodermolides. In preferred embodiments, such compounds have formula XI: ##STR17## where R₃₀ is substituted or unsubstituted C₁ -C₁₀ alkyl or a moiety formula XII or XIII: ##STR18##

where A is C₁ -C₂₀ alkyl, --CH₂ NH(T) or a moiety of formula XIV: ##STR19## wherein T is peptide having 1 to about 10 amino acids;

R₃₂, R₄₀, R₄₂, R₄₃, R₄₆, R₄₇, and R₄₈ are, independently, hydrogen or C₁ -C₆ alkyl;

R₄₁ is a side chain of an amino acid;

W₁ and W₂ are, independently, --OR₄₉ or --NHP₁ ;

P₁ is hydrogen or an amine protecting group;

R₃₃ and R₃₆ are, independently, hydrogen, C₁ -C₁₀ alkyl, --OR₅₀, ═O or together form --CH₂ --CH₂ --;

R₃₄ and R₃₅ are, independently, hydrogen or together form --C(H)═C(H)--C(H)═C(H)--;

R₃₉ is --OR₅₁ or --CH₂ --R₅₁ ;

R₃₁ and R₄₄ are, independently, C₁ -C₁₀ alkyl;

Q₁ and Q₂ are, independently, hydrogen, --OR_(Q), --NHR₅₂, --OC(═O)NH₂ or together form --O--C(O)--NH--;

R_(Q) is hydrogen or a hydroxyl protecting group;

R₅₁ is substituted or unsubstituted C₆ -C₁₄ aryl, tetrahydropyranyl, furanosyl, pyranosyl (e.g., tetramethylfucosyl, tetramethylmannosyl, tetramethylgaractosyl and tetramethylglucosyl), C₃ -C₁₀ lactonyl or 2-pyranonyl;

R₄₅ is C₁ -C₆ alkenyl, C₁ -C₆ alkyl, C₆ -C₁₄ aryl, C₂ -C₁₀ heterocycloalkyl, C₃ -C₁₀ cycloalkyl, or C₇ -C₁₅ aralkyl; and

R₄₉, R₅₀, and R₅₂ are, independently, hydrogen or C₁ -C₆ alkyl.

In another aspect, the present invention provides processes for preparing amides having formula XX: ##STR20## wherein Ar is C₆ -C₁₄ aryl comprising the steps of contacting a compound having formula XXI: ##STR21## with a compound having formula XXII: ##STR22## for a time and under conditions effective to form the amide.

Also provided are processes for producing compounds of formula XXIII: ##STR23## comprising the steps of contacting an aldehyde of formula XXIV: ##STR24## with an enol ether of formula XXV: ##STR25## in the presence of a titanium salt for a time and under conditions effective to form an enone of formula XXVI: ##STR26## Such enones are then contacted with a reducing agent for a time and under conditions effective to form a corresponding enol, which is contacted with a compound having formula R₁₄ --L (wherein L is a leaving group) for a time and under conditions effective to form a protected enol. This protected enol is contacted with an oxidizing agent for a time and under conditions effective to oxidize the carbon-carbon double bond of the protected enol.

The invention also provides processes for producing halogenated olefins of formula XXVII: ##STR27## by contacting an aldehyde of formula XXVIII: ##STR28## with an α-halo sulfone of formula XXIX: ##STR29## for a time and conditions effective to from the halogenated olefin.

Also provided are processes for producing halogenated olefins of formula XXX: ##STR30## comprising the steps of contacting a compound of formula XXXI: ##STR31## with triphenylphosphine and a carbon tetrahalide for a time and under conditions effective to form a dihalogenated olefin of formula XXXII: ##STR32## Such a dihalogenated olefin is contacted with an organometallic compound (such as lithium dimethyl cuprate or an alkylzinc compound such as methyl zinc chloride or methyl zinc bromide) in the presence of a catalyst for a time and under conditions effective to form the halogenated olefin.

Additional processes of the invention are directed to synthesis of dienes of formula XXXIII: ##STR33## comprising contacting a phosphonium salt of formula XXXIV: ##STR34## with a base and a compound of formula XXXV: ##STR35## for a time and under conditions effective to form the diene.

The invention also provides processes for producing a compound of formula XXXVI: ##STR36## comprising contacting a compound of the formula XXXVII: ##STR37## wherein J is C₁ -C₁₀ alkyl, C₆ -C₁₄ aryl, C₂ -C₁₀ heterocycloalkyl. or C₂ -C₁₀ heterocycloalkenyl (preferably 4-methoxyphenyl, 4-hydroxyphenyl, 2-pyridyl, 3-pyridyl, or 4-pyridyl) with a phosphonium salt of formula XXXIV: ##STR38## and base.

The invention also provides synthetic intermediates having formulas XXXIII-XXXXV: ##STR39##

The present invention also provides methods for inhibiting mammalian cell proliferation by contacting mammalian cells with a compound according to the invention or by administering a compound according to the invention (or a pharmaceutical composition comprising such a compound) to a mammal suffering from undesired cell proliferation. Also provided are methods for inhibiting rejection of a transplanted organ in a mammal comprising administering a compound or composition according to the invention to a mammalian organ recipient.

BRIEF DESCRIPTION OF THE DRAWINGS

The numerous objects and advantages of the present invention may be better understood by those skilled in the art by reference to the accompanying figures, in which:

FIG. 1 shows a retrosynthetic analysis for (-)-discodermolide 1.

FIG. 2 shows a synthetic scheme for compound (+)-5.

FIG. 3 shows a synthetic scheme for fragment A.

FIG. 4 shows a synthetic scheme for compound 22.

FIG. 5 shows a synthetic scheme for compound 39.

FIG. 6 shows a synthetic scheme for compounds 15 and 25.

FIG. 7 shows a synthetic scheme for compound 34.

FIG. 8 shows a synthetic scheme for fragment C.

FIG. 9 shows a synthetic scheme for fragment B.

FIG. 10 shows a synthetic scheme for compound 39.

FIG. 11 shows a synthetic scheme for compound 40.

FIG. 12 shows a synthetic scheme for compound 49.

FIG. 13 shows a synthetic scheme for compounds 53 and 46.

FIG. 14 shows a synthetic scheme for compound 56.

FIG. 15 shows a synthetic scheme for compound 1.

FIG. 16 shows a synthetic scheme for compound 104.

FIG. 17 shows a synthetic scheme for compound 107.

FIG. 18 shows asynthetic scheme for compound 206.

FIG. 19 shows a synthetic scheme for compound 212.

FIG. 20 shows asynthetic scheme for compound 217.

FIG. 21 shows a synthetic scheme for compound 305.

FIG. 22 shows a synthetic scheme for compound 309.

FIG. 23 shows a synthetic scheme for compound 401.

FIG. 24 shows asynthetic scheme for compound 501.

FIG. 25 shows a synthetic scheme for compound 601.

FIG. 26 shows a synthetic scheme for compound 701®=alkyl).

FIG. 27 shows a synthetic scheme for compound 808.

FIG. 28 shows a synthetic scheme for compound 801.

FIG. 29 shows asynthetic scheme for compound 901.

FIG. 30 shows a synthetic scheme for compound 1003.

FIG. 31 shows a synthetic scheme for compound 1104 (Ar=2,4-dimethyl-3-methoxyphenyl (a), 2-methyl-5-methoxyphenyl (b), 2,4-dimethyl-5-methoxyphenyl (c), 2,4-dimethylphenyl (d), and 4-methylphenyl (e)).

FIG. 32 shows a synthetic scheme for compound 1111.

FIGS. 33-36 show representative compounds of the invention.

FIG. 37 shows a synthetic scheme for compound (-)-5.

FIG. 38 shows a synthetic scheme for compound 67.

FIG. 39 shows a synthetic scheme for compound (+)-B.

FIG. 40 shows a synthetic scheme for compound 58.

FIG. 41 shows a synthetic scheme for compound 86.

FIG. 42 shows a synthetic scheme for compound 58.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

It has been found in accordance with the present invention that the synthesis of polyhydroxy, dienyl lactones such as the discodermolides can be achieved by highly convergent and stereocontrolled synthetic procedures.

As shown in FIG. 1 for the (-)-discodermolide antipode, our analysis revealed a repeating triad of contiguous stereocenters, separated by Z-olefinic linkages at C(8,9) and C(13,14). Disconnections at C(8,9), C(14,15) and C(21,22) generated fragments A, B and C, each deriving in turn from a common precursor (5) containing the recurring stereochemical triad.

As shown in FIG. 2, precursor 5 was prepared by a synthetic procedure whereby hydroxy ester (-)-6 was protected as the p-methoxybenzyl (PMB) ether by treatment with the Bundle trichloroimidate reagent 7 under acidic conditions. Reduction with LiAlH₄ provided the alcohol (-)-8 after distillation. Swern oxidation, Evans aldol condensation, and Weinreb amide formation completed the construction of common precursor (+)-5. This concise five-step synthesis could be routinely carried out on a 50-g scale in 59% overall yield.

Alternatively, as shown in FIG. 37, Swern oxidation of (+)-8 followed by the addition norephedrine derived oxazolidinone 61 results in a crystalline product 62 which, in turn, can be converted to common precursor (-)-5.

In view of the polypropionate structure of the A fragment, we performed a second asymmetric aldol reaction, as shown in FIG. 3. Initial formation of the p-methoxybenzylidene acetal (-) -11 from common precursor (-)-5 (78% yield) was designed to allow selective deprotection of C(21) and C(19) hydroxyls for introduction of the terminal diene and carbamate moieties. Following reduction of amide (-)-11 to the aldehyde (80% yield), (aldol reaction with oxazolidinone (+)-9 (80% yield) provided alcohol (+)-13 which incorporated the five stereocenters of subunit A. The structure of (+)-13 was confirmed by single-crystal X-ray analysis. Protection of the secondary alcohol as the TBS ether and removal of the chiral auxiliary (LiBH₄,EtOH,THF) afforded primary alcohol (-)-15 (81% yield, two steps), which could be efficiently converted either to tosylate (-)-16 or iodide (-)-A.

As outlined in FIG. 1, our strategy required a Z vinylic halide B for coupling with fragment A. Beginning again with the common precursor (+)-5, TBS protection (FIG. 4) followed by reduction of the Weinreb amide [DIBAL (2 equiv), THF, -78° C.] (Kim, et al., Tetrahedron Lett. 1989, 30, 6697) afforded aldehyde (+)-18 in 88% yield for the two steps. We adopted a stepwise approach to introduction of the vinyl halide, whereby (+)-18 was converted to the Z α-bromo unsaturated ester (-)-19 (Ph₃ PCBrCO₂ Et, PhH, reflux; 75% yield after chromatography). Reduction to allylic alcohol (-)-20 followed by mesylation and displacement with LiBHEt₃ then furnished Z vinyl bromide (-)-22 in 77% overall yield from 19.

One preferred synthetic strategy utilized a vinyl iodide as the desired B segment. Synthesis of (-)-B was achieved by direct olefination of aldehyde (+)-18 (41%, 6:1 Z/E) (FIG. 9), followed by chromatographic removal of the undesired E product. Alternatively, the B segment can be prepared by the two routes shown in FIG. 39. The first involves an α-iodo sulfone 69 to effect a one-step installation of the vinyl iodide. The second exploits the enhanced reactivity of the trans iodide of diiodide 70.

Our preferred synthetic strategy involves selective removal of a primary PMB ether in the presence of a PMP acetal in the AB coupling product ((-)-39, FIG. 5). A 1:1 mixture of PMB ether (-)-22 and PMP acetal (-)-15 was exposed to DDQ (1.1 equiv) in CH₂ Cl₂ /H₂ O (FIG. 6). The acetal (-)-15 largely remained intact while the debenzylated alcohol (-)-25 was formed in 83% yield.

As shown in FIG. 7, we again utilized the TBS ether (+)-17 for the preparation of C from common precursor (+)-5. Oxidative cleavage of the PMB group (DDQ, CH₂ Cl₂, H₂ O) provided alcohol 26 in variable (60-86%) yields, accompanied by the corresponding lactone. Hydrogenolysis with Pearlman's catalyst afforded (+)-26 in 92% yield. Exposure of the alcohol to SO₃.pyr furnished aldehyde (+)-27 (98% yield), which in turn was converted to dithiane (+)-28 (79%). In the latter step, our modification of the Evans protocol for dithiane generation [(TMSSCH₂)₂ CH₂, ZnCl₂, Et₂ O] minimized elimination of the TBS ether to form the α,β-unsaturated amide. Following reduction to aldehyde (+)-29 with DIBAL (91% yield), dimethyl acetal formation gave (+)-30 (99%). The coupling of dithiane 30 with R-(-)-glycidyl benzyl ether [(-)-31] then afforded alcohol (-)-32 in 79% yield. Unmasking of the ketone moiety [(CF₃ CO₂)₂ IPh, 80%] and Evans stereocontrolled reduction (97%) provided the anti diol (-)-34, which embodied all of the stereocenters in fragment C.

Acid-catalyzed cyclization of (-)-34 (TsOH, room temperature) provided methoxy pyran 35 in 87% yield as a 1:2 mixture of α and β anomers (FIG. 8). Debenzylation (H₂, Pd/C) of 36 afforded alcohol 37 quantitatively. Exposure to EtSH and MgBr₂ in Et₂ O then gave a separable 6:1 mixture of β ethyl hemithioacetal (+)-38 and its a anomer in 83% yield. Swern oxidation of (+)-38 furnished the final fragment (+)-C in 86% yield.

Reaction of (-)-B with the organozinc derivative of (-)-A (FIG. 10) was achieved by premixing iodide A with dried solid ZnCl₂ (ether, -78° C.) before addition of t-BuLi. It is believed that three equivalents of t-BuLi are required for complete consumption of (-)-A, probably because the first equivalent reacts with ZnCl₂. This modification increased the yield to 66% after flash chromatography.

Conversion of the Z trisubstituted olefin (-)-39 to the phosphonium iodide (-)-49 began with selective removal of the PMB group, as in our model study (DDQ, CH₂ Cl₂, H₂ O), furnishing (-)-40 in 87% yield (FIG. 11). As shown in FIG. 12, alcohol (-)-40 furnished the requisite iodide 42 almost exclusively, as indicated by NMR examination of the crude material. The very sensitive iodide was used without purification. Thorough mixing of iodide 42 with I-Pr₂ NEt (3 equiv) followed by exposure to excess PPh₃ (15 equiv) without solvent at 80° C. generated (-)-49 in 37% yield for the two steps. The major by-product was characterized as (-)-50 (35% yield). The unsaturated model alcohol (+)-44 similarly afforded the Wittig salt (+)-46 in low yield (FIG. 13), whereas the saturated derivative (+)-51 gave phosphonium iodide (+)-53 almost quantitatively.

Our preferred method to prepare compound 49 entails the mixing of iodide 42 with I-Pr₂ NEt (0.5 equiv.) and PPh₃ (4 equiv.) in benzene/toluene (7:3) and subjecting this mixture to an applied pressure of 10-15 Kbar.

As shown in FIG. 14, assembly of the discodermolide backbone entailed Wittig coupling of aldehyde C with the ylide derived from AB phosphonium salt (-)-49 to install the C(8,9) Z alkene in (-)-54 (>49:1 Z/E, 76% yield). DIBAL reduction (88% yield) followed by oxidation of the resultant primary alcohol (-)-55 then produced aldehyde (-)-56 (96%). The terminal Z diene (-)-57 was elaborated via the Yamamoto protocol in 70% yield with excellent selectivity (16:1 Z/E). After flash chromatography, hydrolysis of the hemithio acetal and mils DMSO/AC₂ O oxidation provided lactone (-)-58 in 82% yield for the two steps. Removal of the PMB group (DDQ, CH₂ Cl₂, H₂ O, 95% yield) and carbamate formation (Cl₃ CONCO, CH₂ Cl₂, neutral Al₂ O.sub.₃, 83%) afforded tris(TBS ether) (-)-60. Final deprotection with 48% HF/CH₃ CN (1:9) furnished (-)-discodermolide, identical with an authentic sample (FIG. 15).

Alternatively, lactone 58 can be prepared by the Wittig coupling of aldehyde 67 with the ylide derived from 49, as shown in FIG. 42. Regioselective ring opening of benzylidene acetal 76 with DIBAL followed by oxidation with pyridinium dichromate affords aldehyde 77. Application of the Yamamoto olefination protocol affords compound 58. Alternatively, the diene installation can be effected using an alkyl chromium reagent generated by the procedure of Hodgson, et al., Tetrahedron Letters 1992, 33, 4761. The aldehyde 67 can be prepared by from compound (-)-27 (prepared generally according to the procedure of Smith, et al., J. Am. Chem. Soc. 1995, 117, 12011) by effecting a Mukaiyama aldol reaction between aldehyde 27 and enol ether 63 to form enone 64. Reduction of enone 64 furnished a 9:1 mixture of carbinols, favoring the desired isomer. Protection of the newly formed carbinol with TBSC and subsequent ozonolysis of the trisubstituted olefin provides 67 in approximately 80% overall yield, as shown in FIG. 38.

Alternatively, the discodermolide backbone can be synthesized by installing the terminal diene before Wittig coupling with Fragment C. As shown in FIG. 40, regioselective ring opening of benzylidine acetal 39 with DIBAL-H followed by oxidation and application of the Yamamoto olefination protocol provides diene 73. Selective removal of the less hindered PMB using DDQ/H₂ O is followed by conversion to the primary iodide and phosphonium salt 75. Alternatively, the primary PMB can be enhanced for either a dimethoxy benzyl ether or silyl protecting group earlier in the sequence. Application of Dauben's high pressure conditions results in approximately 75% yield of the desired phosphonium salt. Further assembly of the discodermolide backbone entails Wittig coupling of aldehyde 67 with the ylide derived from phosphonium salt 75 to afford 58. Further manipulation as indicated above (FIG. 15) provides (+)-discodermolide.

Preferred processes according to the invention also involve contacting a phosphonium salt of formula I with base and an alkylthiol of formula I: ##STR40## to form a diene of formula III: ##STR41## wherein: R₁, R₂, R₃, R₇, R₈, R₁₁, R₁₂ and R₁₃ are, independently, C₁ -C₁₀ alkyl;

X is a halogen;

R₆ is selected from the group consisting of H and C₁ -C₁₀ alkyl;

Z, Z₁, and Z₂ are, independently, O, S or NR';

R₄, R₉, R₁₄, and R₁₅ are, independently, acid labile hydroxyl protecting groups;

R₅ is C₆ -C₁₄ aryl;

Y is O, S or NR';

R' and R₁₆ are, independently, hydrogen or C₁ -C₆ alkyl; and

R₁₈ is C₆ -C₁₄ aryl.

Such procedures preferably are run in solvents such as tetrahydrofuran at -78° C.-0° C. Suitable bases for such procedures include sodium hexamethyldisilazide, potassium hexamethyldisilazide, and n-butyllithium with hexamethylphosphoramide.

Alkyl groups according to the invention include but are not limited to straight chain and branched chain hydrocarbons such as methyl, ethyl, propyl, pentyl, isopropyl, 2-butyl, isobutyl, 2-methylbutyl, and isopentyl moieties having 1 to about 10 carbon atoms, preferably 1 to about 6 carbon atoms. Cycloalkyl groups are cyclic hydrocarbons having 3 to about 10 carbon atoms such as cyclopentyl and cyclohexyl groups. Heterocycloalkyl groups are cycloalkyl groups which include at least one heteroatom (i.e., an atom which is not carbon, such as O, S, or N) in their cyclic backbone. Alkenyl groups according to the invention are straight chain or branched chain hydrocarbons that include one or more carbon-carbon double bonds. Preferred alkenyl groups are those having 2 to about 10 carbon atoms. Alkyl, cycloalkyl, heterocycloalkyl, and alkenyl groups according to the invention optionally can be unsubstituted or can bear one or more substituents such as, for example, halogen hydroxyl, amine, and epoxy groups.

Aryl groups according to the invention are aromatic and heteroaromatic groups having 6 to about 14 carbon atoms, preferably from 6 to about 10 carbon atoms, including, for example, naphthyl, phenyl, indolyl, and xylyl groups and substituted derivatives thereof, particularly those substituted with amino, nitro, hydroxy, methyl, methoxy, thiomethyl, trifluoromethyl, mercaptyl, and carboxy groups. Alkaryl groups are groups that contain alkyl and aryl portions and are covalently bound to other groups through the alkyl portion, as in a benzyl group.

Protecting groups are known per se as chemical functional groups that can be selectively appended to and removed from functionality, such as hydroxyl and amine groups, present in a chemical compound to render such functionality inert to certain chemical reaction conditions to which the compound is exposed. See, e.g., Greene and Wuts, Protective Groups in Organic Synthesis, 2d edition, John Wiley & Sons, New York, 1991. Numerous hydroxyl protecting groups are known in the art, including the acid-labile t-butyldimethylsilyl, diethylisopropylsilyl, and triethylsilyl groups and the acid-stable aralkyl (e.g., benzyl), triisopropylsilyl, and t-butyldiphenylsilyl groups. Useful amine protecting groups include the allyloxycarbonyl (Alloc), benzyloxycarbonyl (CBz), chlorobenzyloxycarbonyl, t-butyloxycarbonyl (Boc), fluorenylmethoxycarbonyl (Fmoc), isonicotinyloxycarbonyl (I-Noc) groups.

Phosphonium salts of formula I can be prepared by reacting a corresponding halogen of formula XXXXVI: ##STR42## with P(R₁₈)₃ in an for a time and under conditions effective to produce the salt. This reaction preferably is conducted in a aromatic hydrocarbon organic solvent such as toluene or benzene. A mixture of benzene and toluene in a ratio of 7:3 is preferred at a pressure of about 5 Kbar to about 20 Kbar.

The methods of the invention involve also are directed to the synthesis of alkenes of formula IV: ##STR43## by contacting organometallic reagents of formula Va: ##STR44## with vinyl halides of formula VIa: ##STR45## wherein M is Li, Cu, Mg, or Zn, and R₁₀ is an acid stable hydroxyl protecting group. Alternatively, a vinyl halide of formula Vb: ##STR46## is contacted with an organometallic compound of formula VIb: ##STR47## Such reactions preferably are performed in the presence of a palladium-containing catalyst such as Pd(PPh₃)₄, Pd(Cl₂) (PPh₃)₂, Pd(Cl₂) (dppf)₂.

In yet another aspect, the synthetic methods of the invention are directed to the preparation of compounds having formula VII: ##STR48## by contacting a diene of formula VIIIa: ##STR49## with an organometallic compound having formula Va wherein R₂₄ is hydrogen and R₂₅ is hydrogen or an acid stable hydroxyl protecting group. Alternatively, an organometallic compound having formula VIIIb is contacted with a vinyl halide having formula Vb. ##STR50## The reaction of compounds having formulas V and VIII preferably is performed in ether in the presence of a palladium- or nickel-containing catalyst.

The methods of the invention also involve producing dienes having formula VIIIa by contacting phosphonium salts having formula IX: ##STR51## with a base such as sodium hexamethyl disilazide and an alkylthiol compound having formula II. Such procedures preferably are run in solvents such as tetrahydrofuran at -78° C.-0° C. Suitable bases for such procedures include sodium hexamethyldisilazide, potassium hexamethyldisilazide, and n-butyllithium with hexamethylphosphoramide.

The methods of the invention also involve producing compounds of formula XXIII: ##STR52## by contacting an aldehyde of formula XXIV: ##STR53## with an enol ether of formula XXV: ##STR54## in the presence of a titanium salt and an organic acid to form an enone of formula XXVI: ##STR55## Preferably, the reaction between aldehyde 27 and the enol ether 62 is a Mukaiyama aldol reaction wherein the Lewis acid is a titanium salt (such as TiCl₄) or some other Ti(IV) of Sn(IV) Lewis acid (such as SnCl₄) and the organic acid is trichloroacetic acid, trifluoroacetic acid, sulfuric acid, or pyridinium p-toluenesulfonate. Following the aldol reaction, enone 64 is contacted with a reducing agent to form the corresponding enol 65. Preferably, the reducing agent is potassium tri-sec-butylborohydride or sodium tri-sec-butylborohydride (commercially available in THF as K-Selectride® and N-Selectride®, respectively) but may include chiral reducing agents such as lithium B-isopinocampheyl-9-borabicyclo[3.3.1]nonyl hydride (commercially available in THF as Alpine-Hydride®.

According to the present invention, enol 65 is then contacted with a compound having formula R₁₄ --L wherein R is an acid labile protecting group and L is a leaving group. Preferably, R₁₄ --L is t-butyldimethylsilyl chloride or t-butyldimethysilyl triflate.

The protected enol is then oxidized with an oxidizing agent such as O₃ or the reagent combination of NaIO₄ with catalytic OsO₄ for a time and under conditions effective to oxidize the carbon-carbon double bond of the protected enol.

The methods of the present invention are also directed to the synthesis of diene having formula XXXIII: ##STR56## by contacting phosphonium salts of formula XXXIV: ##STR57## with base and a compound of formula XXXV: ##STR58## Suitable bases for such procedures include potassium hexamethyldisilazide, sodium hexamethyldisilazide, n-butyllithium and potassium t-butoxide. A preferred solvent is toluene, preferably at a temperature of -78° C.-0° C.

Phosphonium salts of formula XXXIV can be prepared by reacting a corresponding halogen of formula XXXXVII: ##STR59## with P(R₁₈)₃ in an for a time and under conditions effective to produce the salt. This reaction preferably is conducted in a aromatic hydrocarbon organic solvent such as toluene or benzene. A mixture of benzene and toluene in a ratio of 7:3 is preferred at a pressure of about 5 Kbar to about 20 Kbar.

Further processes of the invention involve producing compound having formula XXXVI: ##STR60## by contacting a compound of formula XXXVII: ##STR61## with base and a phosphonium salt of formula XXXIV: ##STR62## Preferred bases include sodium hexamethyldisilazide, potassium hexamethyldisilazide, n-butyllithium with hexamethylphosphoramide, and potassium t-butoxide. A preferred solvent is toluene, preferably at a temperature of -78° C.-0° C.

According to methods of the invention, removal of the acid stable protective group and carbamate formation followed by final deprotection furnishes compounds having formula: ##STR63##

Although preferred synthetic methods are those directed to (+)-discodermolide and compounds having like stereochemistry, those skilled in the art will recognize that the methods disclosed herein can be readily adapted to the synthesis of antipodal compounds such as, for example, (-)-discodermolide, and vice versa. All such synthetic methods are within the scope of the present invention.

The present invention provides compounds which mimic the chemical and/or biological activity of the discodermolides. In preferred embodiments, such compounds have formula XI: ##STR64## where R₃₀ is substituted or unsubstituted C₁ -C₁₀ alkyl or a moiety formula XII or XIII: ##STR65## where A is C₁ -C₂₀ alkyl, --CH₂ NH(T) or a moiety of formula XIV: ##STR66## wherein T is peptide having 1 to about 10 amino acids;

R₃₂, R₄₀, R₄₂, R₄₃, R₄₆, R₄₇, and R₄₈ are, independently, hydrogen or C₁ -C₆ alkyl;

R₄₁ is a side chain of an amino acid;

W₁ and W₂ are, independently, --OR₄₉ or --NHP₁ ;

P₁ is hydrogen or an amine protecting group;

R₃₃ and R₃₆ are, independently, hydrogen, C₁ -C₁₀ alkyl, --OR₅₀, ═O or together form --CH₂ --CH₂ --;

R₃₄ and R₃₅ are, independently, hydrogen or together form --C(H)═C(H)--C(H)═C(H)--;

R₃₉ is --OR₅₁ or --CH₂ --R₅₁ ;

R₃₁ and R₄₄ are, independently, C₁ -C₁₀ alkyl;

Q₁ and Q₂ are, independently, hydrogen, --OR_(Q), --NHR₅₂, --OC(═O)NH₂ or together form --O--C(O)--NH--;

R_(Q) is hydrogen or a hydroxyl protecting group;

R₅₁ is substituted or unsubstituted C₆ -C₁₄ aryl, tetrahydropyranyl, furanosyl, pyranosyl, C₃ -C₁₀ lactonyl or 2-pyranonyl;

R₄₅ is C₁ -C₆ alkenyl, C₁ -C₆ alkyl, C₆ -C₁₄ aryl, C₂ -C₁₀ heterocycloalkyl, C₃ -C₁₀ cycloalkyl, or C₇ -C₁₅ aralkyl; and

R₄₉, R₅₀, and R₅₂ are, independently, hydrogen or C₁ -C₆ alkyl.

Some preferred compounds having formula XI are shown in FIGS. 33-36.

The term amino acid as used herein is intended to include all naturally-occurring and synthetic amino acids known in the art. In general, amino acids have structure H₂ N--CH(R_(c))--C(O)OH where R_(c) is the amino acid side chain. Representative, naturally-occurring side chains are shown in Table 1.

                                                      TABLE 1                 

    ______________________________________                                         CH.sub.3 --                                                                      HO--CH.sub.2 --                                                                C.sub.6 H.sub.5 -- CH.sub.2 --                                                 HO--C.sub.6 H.sub.5 -- CH.sub.2 --                                              -                                                                             #STR67##                                                                        -                                                                             #STR68##                                                                        -                                                                             #STR69##                                                                        - HS--CH.sub.2 --                                                             HO.sub.2 C--CH(NH.sub.2)--CH.sub.2 --S--S--CH.sub.2 --                         CH.sub.3 --CH.sub.2 --                                                         CH.sub.3 --S--CH.sub.2 --CH.sub.2 --                                           CH.sub.3 --CH.sub.2 --S--CH.sub.2 --CH.sub.2 --                                HO--CH.sub.2 --CH.sub.2 --                                                     CH.sub.3 --CH.sub.2 (OH)--                                                     HO.sub.2 C--CH.sub.2 --NH.sub.2 C(O)--CH.sub.2 --                               -                                                                             #STR70##                                                                        - HCO.sub.2 --CH.sub.2 --CH.sub.2 --                                          NH.sub.2 C(O)--CH.sub.2 --CH.sub.2 --                                          (CH.sub.3).sub.2 --CH--                                                        (CH.sub.3).sub.2 --CH--CH.sub.2 --                                             CH.sub.3 --CH.sub.2 --CH.sub.2 --                                              H.sub.2 N--CH.sub.2 --CH.sub.2 --CH.sub.2 --                                   H.sub.2 N--C(NH)--NH--CH.sub.2 --CH.sub.2 --CH.sub.2 --                        H.sub.2 N--C(O)--NH--CH.sub.2 --CH.sub.2 --CH.sub.2 --                         CH.sub.3 --CH.sub.2 --CH(CH.sub.3)--                                           CH.sub.3 --CH.sub.2 --CH.sub.2 --CH.sub.2 --                                   H.sub.2 N--CH.sub.2 --CH.sub.2 --CH.sub.2 --CH.sub.2 --                      ______________________________________                                    

Hydrophobic amino acid side chains are preferred, including the CH₃ --, C₆ H₅ --CH₂ --, CH₃ --CH₂ --, CH₃ --S--CH₂ --CH₂ --, (CH₃)₂ --CH--, (CH₃)₂ --CH--CH₂ --, CH₃ --CH₂ --CH(CH₃)--, and CH₃ --CH₂ --CH₂ --CH₂ -- side chains. Peptides according to the invention are linear, branched, or cyclic chemical structures containing at least 2 covalently bound amino acids.

Certain compounds of the invention contain amino groups and, therefore, are capable of forming salts with various inorganic and organic acids. Such salts are also within the scope of this invention. Representative salts include acetate, adipate, benzoate, benzenesulfonate, bisulfate, butyrate, citrate, camphorate, camphorsulfonate, ethanesulfonate, fumarate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, methanesulfonate, lactate, maleate, methanesulfonate, 2-naphthalenesulfonate, nitrate, oxalate, pamoate, persulfate, picrate, pivalate, propionate, succinate, sulfate, tartrate, tosylate, and undecanoate. The salts can be formed by conventional means, such as by reacting the free base form of the product with one or more equivalents of the appropriate acid in a solvent or medium in which the salt is insoluble, or in a solvent such as water which is later removed in vacuo or by freeze drying. The salts also can be formed by exchanging the anions of an existing salt for another anion on a suitable ion exchange resin.

The compounds of the invention can be admixed with carriers, excipients, and/or diluents to form novel compositions. Such compositions can be used in prophylactic, diagnostic, and/or therapeutic techniques. By administering an effective amount of such a composition, prophylactic or therapeutic responses can be produced in a human or some other type mammal. It will be appreciated that the production of prophylactic or therapeutic responses includes the initiation or enhancement of desirable responses, as well as the mitigation, cessation, or suppression of undesirable responses. The compositions of the invention are expected to find use, for example, in the inhibition of undesired cell proliferation (e.g., cancer) and in the inhibition of rejection in organ transplantation procedures. (See, e.g., Longley, et al., Transplantation 1991, 52, 650 and 656).

Compositions of the invention can be prepared by any of the methods well known in the pharmaceutical art, for example, as described in Remington's Pharmaceutical Sciences (Mack Pub. Co., Easton, Pa., 1980). The compositions can include a compound of the invention as an active ingredient in admixture with an organic or inorganic carrier or excipient suitable, for example, for oral administration. Other suitable modes of administration will be apparent to those skilled in the art. The compound of the invention can be compounded, for example, with the usual non-toxic, pharmaceutically acceptable carriers for tablets, pellets, capsules, solutions, suppositories, suspensions, and any other form suitable for use. The carriers which can be used are water, glucose, lactose, gum acacia, gelatin, mannitol, starch paste, magnesium trisilicate, talc, corn starch, keratin, colloidal silica, potato starch, urea and other carriers suitable for use in manufacturing preparations, in solid, semisolid, or liquid form, and in addition auxiliary, stabilizing, thickening and coloring agents and perfumes may be used. The compound of the invention is included in the pharmaceutical composition in an amount sufficient to produce the desired effect upon the process or condition of diseases.

For oral administration, tablets containing various excipients such as microcrystalline cellulose, sodium citrate, calcium carbonate, dicalcium phosphate and glycine may be employed along with various disintegrants such as starch and preferably corn, potato or tapioca starch, alginic acid and certain complex silicates, together with granulation binders like polyvinylpyrrolidone, sucrose, gelatin and acacia. Additionally, lubricating agents such as magnesium stearate, sodium lauryl sulfate and talc are often very useful for tableting purposes. Solid compositions of a similar type may also be employed as fillers in appropriately soluble (e.g., gelatin) capsules; preferred materials in this connection also include lactose or milk sugar as well as high molecular weight polyethylene glycols.

When aqueous suspensions and/or elixirs are desired for oral administration, the active ingredient may be combined with various sweetening or flavoring agents, coloring matter or dyes, and, if so desired, emulsifying and/or suspending agents as well, together with such diluents as water, ethanol, glycerin and various like combinations thereof.

For parenteral administration, suspensions containing a compound of the invention in, for example, aqueous propylene glycol can be employed. The suspensions should be suitably buffered (preferably pH>8) if necessary and the liquid diluent first rendered isotonic. The aqueous suspensions are suitable for intravenous injection purposes. The preparation of such suspensions under sterile conditions is readily accomplished by standard pharmaceutical techniques well-known to those skilled in the art. Additionally, it is possible to administer the compounds of the invention topically and this may preferably be done by way of creams, jellies, gels, pastes, ointments and the like, in accordance with standard pharmaceutical practice.

The compounds of the invention can be employed as the sole active agent in a pharmaceutical composition or can be used in combination with other active ingredients, e.g., other agents useful in diseases or disorders.

The amount of active ingredient that is to be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration. The specific dose level for any particular patient will depend on a variety of factors including the activity of the specific compound employed, the age, body weight, general health, sex, diet, time of administration, route of administration, rate of excretion, drug combination, and the severity of the particular disease undergoing therapy. In some instances, dosage levels below the lower limit of the aforesaid range may be more than adequate, while in other cases still larger doses may be employed without causing any harmful side effects provided that such higher dose levels are first divided into several small doses for administration throughout the day. The concentrations of the active ingredient in therapeutic compositions will vary depending upon a number of factors, including the dosage of the drug to be administered, the chemical characteristics (e.g., hydrophobicity) of the active ingredient, and the route of administration. Typical dose ranges are from about 285 μg/kg of body weight per day in three divided doses; a preferred dose range is from about 42 μg/kg to about 171 μg/kg of body weight per day. The preferred dosage to be administered is likely to depend on such variables as the type and extent of progression of the disease or disorder, the overall health status of the particular patient, the relative biological efficacy of the compound selected, and formulation of the compound excipient, and its route of administration, as well as other factors, including bioavailability, which is in turn influenced by several factors well known to those skilled in the art.

Additional objects, advantages, and novel features of this invention will become apparent to those skilled in the art upon examination of the following examples thereof, which are not intended to be limiting.

All reactions were carried out in oven-dried or flame-dried glassware under an argon atmosphere, unless otherwise noted. All solvents were reagent grade. Diethyl ether and tetrahydrofuran (THF) were freshly distilled from sodium/benzophenone under argon before use. Dichloromethane, benzene and diisopropyl amine were freshly distilled from calcium hydride before use. Triethylamine and diisopropylethylamine were distilled from calcium hydride and stored over potassium hydroxide. Hexamethylphosphoramide was freshly distilled from calcium hydride. Anhydrous pyridine, dimethylformamide and dimethyl sulfoxide were purchased from Aldrich and used without purification. n-Butyllithium and t-butyllithium were purchased from Aldrich and standardized by titration with diphenylacetic acid.

Unless stated otherwise all reactions were magnetically stirred and monitored by thin layer chromatography using 0.25 mm E. Merck pre-coated silica gel plates. Flash column chromatography was performed with the indicated solvents using silica gel-60 (particle size 0.040-0.062 mm) supplied by E. Merck. Yields refer to chromatographically and spectroscopically pure compounds, unless otherwise stated.

All melting points were determined on a Bristoline heated-stage microscope or a Thomas-Hoover apparatus and are corrected. The IR and NMR were obtained for CHCl₃ and CDCl₃ solutions respectively unless otherwise noted. Infrared spectra were recorded with a Perkin-Elmer Model 283B spectrometer using polystyrene as an external standard. Proton NMR spectra were recorded on a Bruker AM-500 spectrometer. Carbon-13 NMR spectra were recorded on a Bruker AM-500 or AM-250 spectrometer. Chemical shifts are reported relative to internal tetramethylsilane (d 0.00) for proton and chloroform δ77.0) or benzene (δ128.0) for carbon-13. Optical rotations were obtained with a Perkin-Elmer model 241 polarimeter in the solvent indicated. High-resolution mass spectra were obtained at the University of Pennsylvania Mass Spectrometry Service Center on either a VG micromass 70/70H high resolution double-focusing electron impact/chemical ionization spectrometer or a VG ZAB-E spectrometer. Microanalyses were performed by Robertson Laboratories, Madison, N.J. Single-crystal X-ray diffraction structure determination were performed at the University of Pennsylvania using an Enraf Nonius CAD-4 automated diffractometer. High performance liquid chromatography (HPLC) was performed using a Ranin component analytical/semi-prep system.

EXAMPLE 62 Alcohol (-)-8

p-Methoxybenzyl alcohol (200 g, 1.45 mol) was added to a suspension of NaH (60% in mineral oil; 5.82 g, 0.146 mol) in anhydrous ether (450 mL) over 1 h at room temperature. The mixture was stirred for 1 h and cooled to 0° C. Trichloroacetonitrile (158 mL, 1.58 mol) was then introduced over 80 min. After 1.5 h the solution was concentrated with the water bath temperature maintained below 40° C. The residue was treated with a mixture of pentane (1.5 L) and MeOH (5.6 mL), stirred at room temperature for 30 min, and filtered through a short Celite column. Concentration gave the trichloroimidate (394.3 g) as a red oil which was used without further purification.

A solution of (R)-(-)-Roche ester (124.7 g, 1.06 mol) in CH₂ Cl₂ /cyclohexane (1:2, 1.5 L) was cooled to 0° C. and treated with trichloroimidate (364.3 g) and PPTS (13.3 g, 52.9 mmol). After 3 h, the mixture was warmed to room temperature, stirred for 40 h, and concentrated. Filtration through a short silica column (20% ethyl acetate/hexane) afforded the ester (303.5 g) as a slight yellow oil.

The ester (303.5 g) was divided into three portions for the next reaction. In each preparation, solution of crude ester (112.8 g) in anhydrous THF (1.0 L) was cooled to 0° C. and LiAlH₄ (1.0 M in THF, 560 mL, 0.560 mol) was added over 1 h. The mixture was warmed gradually to room temperature and stirred for 24 h. After dilution with ether (1.0 L) the mixture was cooled to 0° C. and quenched carefully with saturated aqueous Rochelle's salt (20 mL). The resultant mixture was then transferred to a 4-L flask, diluted with ether (1.0 L), and treated with additional Rochelle's solution (ca. 300 mL) with shaking until a solid precipitated. The solution was filtered, concentrated, and the residue (including the aqueous layer) was diluted with ether (700 mL), dried over Na₂ SO₄, filtered and concentrated. The crude products of the three reactions were combined and distilled under vacuum, furnishing (-)-8 (142.7 g, 74% yield for two steps) as a colorless oil: [α]²³ _(D) -16.9° ©1.28, CHCl₃); IR (CHCl₃) 3510 (m), 3015 (s), 2965 (s), 2940 (s), 2920 (s), 2870 (s), 2840 (m), 1618 (s), 1590 (m), 1517 (s), 1470 (s), 1445 (m), 1423 (m), 1365 (m), 1305 (s), 1250 (s), 1178 (s), 1092 (s), 1037 (s), 826 (m), 814 (m), 718 (w), 710 (w) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.23 (d, J=8.6 Hz, 2 H), 6.86 (d, J=8.6 Hz, 2 H), 4.43 (ABq, J_(AB) =11.7 Hz, Δδ_(AB) =13.2 Hz, 2 H), 3.78 (s, 3 H), 3.61-3.54 (m, 2 H), 3.53 (ddd, J=9.1, 4.7, 0.8 Hz, 1 H), 3.38 (dd, J=9.1, 7.9 Hz, 1 H), 2.60 (br s, 1 H), 2.08-1.98 (m, 1 H), 0.90 (d, J=7.0 Hz, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.2, 130.2, 129.2, 113.8, 75.0, 73.0, 67.7, 55.2, 35.6, 13.4; high resolution mass spectrum (CI, NH₃) m/z 210.1252 [M⁺ ; calcd for C₁₂ H₁₈ O₃ : 210.1256].

Anal. Calcd for C₁₂ H₁₈ O₃ : C, 68.54; H, 8.63. Found: C, 68.41; H, 8.60.

EXAMPLE 2 Aldol (+)-10

A solution of DMSO (40.0 mL, 564 mmol) in CH₂ Cl₂ (1.0 L) was cooled to -78° C. and oxalyl chloride (23.0 mL, 263 mmol) was added over 1 h. After an additional 15 min, a cooled (-78° C.) solution of alcohol (-)-8 (38.0 g, 181 mmol) in CH₂ Cl₂ (50 mL) was introduced via a cannula over 15 min (20 mL rinse) and the resultant milky mixture was stirred 0.5 h further at -78° C. I-Pr₂ NEt (150 mL, 861 mmol) was then added over 15 min. The mixture was stirred for 30 min, slowly warmed to room temperature (70 min), and quenched with aqueous NaHSO₄ (1.0 M, 1.0 L). The organic phase was concentrated, diluted with ether (500 mL), washed with water (6×500 mL), dried over MgSO₄, filtered and concentrated to give the corresponding aldehyde (38.0 g) as a colorless oil.

A solution of oxazolidinone (+)-9 (44.3 g, 190 mmol) in CH₂ Cl₂ (500 mL) was cooled to 0° C. n-Bu₂ BOTf (1.0 M in CH₂ Cl₂, 199.0 mL, 199 mmol) was introduced over 0.5 h, followed by addition of NEt₃ (30.2 mL, 217 mmol) over 10 min. The mixture was stirred at 0° C. for 0.5 h and cooled to -78° C. A precooled (-78° C.) solution of the above aldehyde in CH₂ Cl₂ (100 mL) was then added via a cannula over 30 min (2×20 mL rinse). After 2 h at -78° C. and 2 h at 0° C., the reaction was quenched with pH 7 phosphate buffer (200 mL). The mixture was slowly treated with a solution of 30% H₂ O₂ in MeOH (1:2, 600 mL) at 0° C., stirred overnight at room temperature, and concentrated. The residue was extracted with ethyl acetate (3×250 mL) and the combined extracts were washed with saturated aqueous NaHCO₃ and water (500 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (30% ethyl acetate/hexane) provided (+)-10 (70.9 g, 89% yield from 8) as a colorless oil: [α]²³ _(D) +278° ©0.49, CHCl₃); IR (CHCl₃) 3470 (w, br), 3020 (m), 2980 (m), 2940 (m), 2920 (m), 2880 (m), 1790 (s), 1705 (m), 1620 (m), 1590 (w), 1520 (m), 1485 (w), 1460 (m), 1390 (m), 1360 (m), 1305 (w), 1230 (br, s), 1110 (m), 1080 (m), 1035 (m), 985 (m), 970 (m), 820 (w), 695 (w) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.33-7.30 (m, 2 H), 7.27-7.19 (m, 5 H), 6.85 (d, J=8.7 Hz, 2 H), 4.67-4.63 (m, 1 H), 4.42 (apparent s, 2 H), 4.14 (apparent d, J=5.0 Hz, 2 H), 3.93 (qd, J=6.9, 3.4 Hz, 1 H), 3.85 (ddd, J=8.2, 3.1, 3.1 Hz, 1 H), 3.78 (s, 3 H), 3.69 (d, J=2.8 Hz, 1 H), 3.54 (apparent t, J=9.3 Hz, 1 H), 3.54 (dd, J=21.1, 9.2 Hz, 1 H), 3.28 (dd, J=13.4, 3.2 Hz, 1 H), 2.76 (dd, J=13.4, 9.6 Hz, 1 H), 1.98-1.93 (m, 1 H), 1.25 (d, J=6.9 Hz, 3 H), 0.94 (d, J=7.0 Hz, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 176.1, 159.2, 153.0, 135.3, 129.9, 129.3, 129.2, 128.8, 127.2, 113.7, 75.3, 74.5, 73.1, 66.0, 55.5, 55.2, 40.6, 37.7, 35.9, 13.5, 9.7; high resolution mass spectrum (CI, NH₃) m/z 442.2243 [(M+H)⁺ ; calcd for C₂₅ H₃₂ NO₆ : 442.2229].

Anal. Calcd for C₂₅ H₃₁ NO₆ : C, 68.01; H, 7.08. Found: C, 67.81; H, 7.26.

EXAMPLE 3 Common Precursor (+)-5

A suspension of N,O-Dimethylhydroxylamine hydrochloride (46.9 g, 481 mmol) in THF (250 mL) was cooled to 0° C. and AlMe₃ (2.0 M in hexane, 240 mL, 480 mmol) was added over 30 min. The resultant solution was warmed to room temperature, stirred for 0.5 h and then cooled to -30° C. A solution of oxazolidinone (+)-10 (70.9 g, 161 mmol) in THF (150 mL) was introduced over 20 min via cannula (20 mL rinse). After 3 h, the solution was poured slowly into a mixture of aqueous HCl (1.0 N, 1.2 L) and CH₂ Cl₂ (1.0 L) at 0° C. and the mixture was shaken vigorously for 1 h. The aqueous phase was extracted with CH₂ Cl₂ (2×500 mL) and the combined organic extracts were washed with water (3×1.0 L), dried over MgSO₄, filtered and concentrated. The crude material was taken up in ethyl acetate/hexane (1:3, 150 mL) with vigorous stirring to precipitate most of the chiral auxiliary. Filtration, concentration and flash chromatography (20% acetone/hexane) afforded (+)-5 (46.2 g, 88% yield) as a colorless oil: [α]²³ _(D) +144° ©0.41, CHCl₃); IR (CHCl₃) 3470 (m, br), 3010 (s), 2975 (s), 2945 (s), 2915 (s), 2870 (s), 2845 (m), 1680 (s), 1590 (w), 1515 (s), 1465 (s), 1425 (m), 1390 (m), 1365 (m), 1310 (m), 1250 (s), 1180 (s), 1150 (m), 1090 (s), 1040 (s), 1000 (s), 825 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.25 (d, J=8.6 Hz, 2 H), 6.86 (d, J=8.7 Hz, 2 H), 4.44 (ABq, J_(AB) =11.6 Hz, Δδ_(AB) =17.1 Hz, 2 H), 3.95 (d, J=2.8 Hz, 1 H), 3.79 (s, 3 H), 3.70 (ddd, J=8.2, 3.2, 3.2 Hz, 1 H), 3.66 (s, 3 H), 3.62 (dd, J=9.0, 4.0 Hz, 1 H), 3.53 (dd, J=9.1, 5.9 Hz, 1 H), 3.17 (s, 3 H), 3.04 (m, 1 H), 1.91-1.84 (m, 1 H), 1.17 (d, J=7.0 Hz, 3 H), 0.98 (d, J=6.9 Hz, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 178.0, 159.0, 130.6, 129.1, 113.7, 113.6, 73.8, 72.8, 72.6, 61.3, 55.1, 36.5, 36.0, 14.2, 10.4; high resolution mass spectrum (CI, NH₃) m/z 326.1962 [(M+H)⁺ ; calcd for C₁₇ H₂₈ NO₅ : 326.1967].

Anal. Calcd for C₁₇ H₂₇ NO₅ : C, 62.74; H, 8.36. Found: C, 62.74; H, 8.24.

EXAMPLE 4 Weinreb Amide (-)-11

A mixture of common precursor (+)-5 (337.3 mg, 1.04 mmol), 4 Å molecular sieves (344 mg), and CH₂ Cl₂ (10 mL) was cooled to 0° C. and treated with DDQ (310.3 mg, 1.37 mmol). After 1.5 h, the mixture was filtered through a short Celite column (50% ethyl acetate/hexane). The filtrate was washed with saturated aqueous NaHCO₃ and water (100 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (30% ethyl acetate/hexane) provided (-)-11 (255.6 mg, 76% yield) as a colorless oil: [α]²³ _(D) -339° ©0.520, CHCl₃); IR (CHCl₃) 3010 (s), 2970 (s), 2940 (m), 2880 (m), 2840 (m), 1663 (s), 1620 (s), 1592 (w), 1520 (s), 1466 (s), 1447 (m), 1425 (m), 1393 (s), 1375 (s), 1307 (m), 1253 (s), 1178 (s), 1120 (s), 1083 (s), 1035 (s), 1015 (m), 1000 (s), 930 (w), 830 (m), 700 (w), 660 (w), 620 (w) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.41 (d, J=8.8 Hz, 2 H), 6.87 (d, J=8.8 Hz, 2 H), 5.46 (s, 1 H), 4.04 (dd, J=11.3, 4.7 Hz, 1 H), 3.82 (dd, J=9.8, 6.5 Hz, 1 H), 3.79 (s, 3 H), 3.71 (s, 3 H), 3.51 (apparent t, J=11.2 Hz, 1 H), 3.19 (s, 3 H), 3.21-3.14 (m, 1 H), 1.98-1.92 (m, 1 H), 1.27 (d, J=7.0 Hz, 3 H), 0.75 (d, J=6.8 Hz, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 175.8, 159.8, 131.2, 127.2, 113.5, 100.7, 82.8, 72.8, 61.3, 55.3, 39.0, 33.8, 32.6, 13.1, 12.4; high resolution mass spectrum (CI, NH₃) m/z 323.1736 [M⁺ ; calcd for C₁₇ H₂₅ NO₅ : 323.1732].

Anal. Calcd for C₁₇ H₂₅ NO₅ : C, 63.14; H, 7.79. Found: C, 63.18; H, 7.74.

EXAMPLE 5 Aldehyde (-)-12

A solution of amide (-)-11 (2.07 g, 6.40 mmol) in THF (70 mL) was cooled to -78° C. and LiAlH₄ (1.0 M in THF, 3.40 mL, 3.40 mmol) was added over 15 min. After 10 min at -78° C. and 10 min at 0° C., the mixture was quenched with MeOH (1.0 mL), and partitioned between ethyl acetate and saturated aqueous Rochelle's salt (100 mL each). The organic phase was washed with brine (100 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (15% ethyl acetate/hexane) gave (-)-12 (1.38 g, 80% yield) as a colorless oil: [α]²³ _(D) -7.8° ©0.46, CHCl₃); IR (CHCl₃) 3015 (m), 2970 (m), 2940 (m), 2840 (m), 1735 (s), 1725 (s), 1615 (m), 1590 (w), 1520 (s), 1460 (s), 1390 (m), 1370 (m), 1305 (m), 1250 (s), 1170 (s), 1115 (s), 1085 (s), 1035 (s), 990 (m), 960 (m), 830 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 9.74 (apparent s, 1 H), 7.32 (d, J=8.8 Hz, 2 H), 6.84 (d, J=8.7 Hz, 2 H), 5.46 (s, 1 H), 4.13 (dd, J=11.5, 4.8 Hz, 1 H), 4.05 (dd, J=10.4, 2.6 Hz, 1 H), 3.77 (s, 3 H), 3.56 (apparent t, J=11.1 Hz, 1 H), 2.56 (qd, J=7.1, 2.6 Hz, 1 H), 2.15-2.03 (m, 1 H), 1.23 (d, J=7.1 Hz, 3 H), 0.80 (d, J=6.7 Hz, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 204.0, 159.9, 130.7, 127.2, 113.5, 100.9, 81.6, 72.8, 55.2, 47.4, 30.3, 11.9, 7.1; high resolution mass spectrum (CI, NH₃) m/z 265.1432 [(M+H)⁺ ; calcd for C₁₅ H₂₁ O₄ : 265.1439].

EXAMPLE 6 Aldol (+)-13

A solution of oxazolidinone (+)-9 (21.6 g, 92.7 mmol) in CH₂ Cl₂ (200 mL) was cooled to 0° C. and n-Bu₂ BOTf (1.0 M in CH₂ Cl₂, 86.1 mL, 86.1 mmol) was added over 0.5 h, followed by addition of NEt₃ (15.7 mL, 112.5 mmol) over 10 min. The mixture was stirred at 0° C. for 1 h and cooled to -78° C. A solution of aldehyde (-)-12 (17.5 g, 66.2 mmol) in CH₂ Cl₂ (50 mL) was added over 10 min. After additional 20 min at -78 ° C. and 1 h at 0 ° C., the reaction was quenched with pH 7 phosphate buffer (100 mL) and MeOH (300 mL), then slowly treated with a solution of 30% H₂ O₂ in MeOH (1:1, 100 mL) at 0° C. After 1 h, saturated aqueous Na₂ S₂ O₃ (100 mL) was added. The mixture was concentrated and the residue was extracted with ethyl acetate (3'250 mL). The combined extracts were washed with saturated aqueous Na₂ S₂ O₃, aqueous NaHCO₃ (10%), brine (200 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (10% ethyl acetate/hexane) provided (+)-13 (26.3 g, 80% yield) as white crystals: mp 98-100° C.; [α]²³ _(D) +13.5° ©1.19, CHCl₃); IR (CHCl₃) 3690 (w), 3520 (w, br), 3020 (m), 2980 (m), 2940 (m), 2880 (w), 2850 (m), 1790 (s), 1695 (m), 1620 (m), 1595 (w), 1525 (m), 1505 (w), 1490 (w), 1465 (m), 1390 (s), 1365 (m), 1310 (m), 1260-1210 (m, br), 1175 (m), 1120 (s), 1085 (m), 1040 (m), 1020 (m), 985 (m), 970 (m), 930 (w), 830 (m), 700 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.35 (d, J=8.7 Hz, 2 H), 7.31 (d, J=7.6 Hz, 2 H), 7.27 (d, J=7.2 Hz, 1 H), 7.19 (d, J=7.7 Hz, 2 H), 6.84 (d, J=8.7 Hz, 2 H), 5.45 (s, 1 H), 4.67-4.62 (m, 1 H), 4.14 (apparent d, J=5.3 Hz, 2 H), 4.08 (dd, J=11.4, 4.8 Hz, 1 H), 4.07 (apparent t, J=4.1 Hz, 1 H), 4.04-3.99 (m, 1 H), 3.76 (s, 3 H), 3.61 (dd, J=9.9, 2.2 Hz, 1 H), 3.51 (apparent t, J=11.1 Hz, 1 H), 3.33 (d, J=1.3 Hz, 1 H), 3.21 (dd, J=13.4, 3.4 Hz, 1 H), 2.76 (dd, J=13.4, 9.4 Hz, 1 H), 2.12-2.06 (m, 1 H), 1.92-1.86 (m, 1 H), 1.31 (d, J=6.9 Hz, 3 H), 1.07 (d, J=7.0 Hz, 3 H), 0.74 (d, J=6.7 Hz, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 177.1, 160.0, 152.7, 135.0, 131.0, 129.4, 128.9, 127.40, 127.39, 113.6, 101.2, 85.8, 74.5, 73.0, 66.0, 55.2, 54.9, 39.8, 37.7, 35.7, 30.4, 12.8, 11.7, 7.8; high resolution mass spectrum (CI, NH₃) m/z 497.2410 [M⁺ ; calcd for C₂₈ H₃₅ NO₇ : 497.2413].

Anal. Calcd for C₂₆ H₃₅ NO₇ : C, 67.58; H, 7.09. Found: C, 67.42; H, 7.02.

EXAMPLE 7 Acetal (+)-14

A solution of alcohol (+)-13 (26.3 g, 52.9 mmol) and 2,6-lutidine (11.1 mL, 95.3 mmol) in CH₂ Cl₂ (150 mL) was cooled to -20° C. and TBSOTf (20.5 mL, 79.3 mmol) was added over 30 min. After additional 2 h at 0° C., the mixture was diluted with ether (300 mL), washed with aqueous NaHSO₄ (1.0 M, 200 mL), brine (200 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (gradient elution, 5%->10% ethyl acetate/hexane) afforded (+)-14 (32.4 g, 100% yield) as a colorless oil: [α]²³ _(D) +20.3° ©1.32, CHCl₃); IR (CHCl₃) 3025 (m), 2970 (m), 2940 (m), 2864 (m), 1788 (s), 1705 (m), 1620 (m), 1597 (w),1524 (m), 1503 (w), 1470 (m), 1447 (w), 1430 (w), 1395 (s), 1358 (m), 1307 (m), 1255 (s), 1135 (m), 1120 (s), 1075 (m), 1030 (m), 985 (m), 976 (m), 930 (m), 865 (m), 838 (s), 813 (m), 790 (m), 700 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.38 (d, J=8.7 Hz, 2 H), 7.30-7.12 (m, 5 H), 6.82 (d, J=8.7 Hz, 2 H), 5.44 (s, 1 H), 4.30 (dddd, J=13.4, 7.3, 5.1, 5.1 Hz, 1 H), 4.11 (dd, J=7.1, 4.0 Hz, 1 H), 4.02 (dd, J=11.2, 4.7 Hz, 1 H), 3.97 (dq, J=7.0, 7.0 Hz, 1 H), 3.80 (dd, J=8.9, 2.3 Hz, 1 H), 3.740 (apparent t, J=4.9 Hz, 1 H), 3.738 (s, 3 H), 3.48 (apparent t, J=11.1 Hz, 1 H), 3.27 (apparent t, J=8.2 Hz, 1 H), 3.15 (dd, J=13.4, 3.2 Hz, 1 H), 2.59 (dd, J=13.4, 9.8 Hz, 1 H), 2.05 (apparent qd, J=7.4, 4.2 Hz, 1 H), 2.02-1.94 (m, 1 H), 1.19 (d, J=6.9 Hz, 1 H), 1.04 (d, J=7.5 Hz, 3 H), 0.92 (s, 9 H), 0.73 (d, J=6.7 Hz, 3 H), 0.05 (s, 3 H), 0.04 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 175.6, 159.9, 152.4, 135.5, 132.0, 129.4, 128.8, 127.8, 127.2, 113.4, 100.7, 80.7, 74.6, 73.1, 65.3, 55.3, 55.2, 41.4, 40.9, 37.4, 30.6, 26.0, 18.1, 15.0, 12.7, 11.5, -4.0, -4.6; high resolution mass spectrum (CI, NH₃) m/z 612.3340 [(M+H)⁺ ; calcd for C₃₄ H₅₀ NO₇ Si: 612.3356].

Anal. Calcd for C₃₄ H₄₉ NO₇ Si: C, 66.74; H, 8.07. Found: C, 66.69; H, 7.98.

EXAMPLE 8 Alcohol (-)-15

A solution of acetal (+)-14 (32.0 g, 52.3 mmol) in THF (600 mL) was cooled to -30° C. and EtOH (6.14 mL, 105 mmol) was added, followed by addition of LiBH₄ (2.0 M in THF, 52.3 mL, 105 mmol) over 15 min. After additional 1 h at 0° C. and 12 h at room temperature, the mixture was diluted with ether (1.0 L), quenched carefully with aqueous NaOH (1.0 N, 200 mL) and stirred for 2 h at room temperature. The layers were separated and the organic phase was washed with brine (500 mL), dried over Na₂ SO₄, filtered and concentrated. Flash chromatography (20% ethyl acetate/hexane) provided (-)-15 (18.7 g, 81% yield) as a colorless oil: [α]²³ _(D) -36.1° ©1.15, CHCl₃); IR (CHCl₃) 3630 (w), 3480 (w, br), 3010 (m), 2960 (s), 2940 (s), 2885 (m), 2860 (s), 1620 (m), 1594 (w), 1523 (s), 1468 (s), 1445 (w), 1430 (w), 1395 (m), 1365 (m), 1307 (m), 1255 (s), 1175 (m), 1165 (m),1150 (m), 1120 (s), 1080 (s), 1030 (s), 990 (m), 968 (m), 910 (s), 860 (m), 833 (s), 700 (m), 645 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.36 (d, J=8.7 Hz, 2 H), 6.85 (d, J=8.8 Hz, 2 H), 5.38 (s, 1 H), 4.08 (dd, J=11.2, 4.7 Hz, 1 H), 3.84 (dd, J=6.7, 1.9 Hz, 1 H), 3.77 (s, 3 H), 3.53 (dd, J=9.9, 1.8 Hz, 1 H), 3.55-3.52 (m, 1 H), 3.47 (apparent t, J=11.1 Hz, 1 H), 3.44 (dd, J=10.3, 6.2 Hz, 1 H), 2.08-1.97 (m, 2 H), 1.94 (dqd, J=7.1, 7.1, 1.7 Hz, 1 H), 1.76 (br s, 1 H), 1.02 (d, J=7.1, 3 H), 0.88 (s, 9 H), 0.84 (d, J=6.9 Hz, 3 H), 0.73 (d, J=6.7 Hz, 3 H), 0.03 (s, 3 H), 0.00 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.8, 131.4, 127.3, 113.5, 101.0, 82.9, 74.3, 73.3, 66.3, 55.2, 38.7, 37.8, 30.7, 26.1, 18.3, 12.2, 11.1, 10.7, -4.0, -4.2; high resolution mass spectrum (CI, NH₃) m/z 439.2889 [(M+H)⁺ ; calcd for C₂₄ H₄₃ O₅ Si: 439.2879].

Anal. Calcd for C₂₄ H₄₂ O₅ Si: C, 65.71; H, 9.65. Found: C, 65.51; H 9.54.

EXAMPLE 9 Tosylate (-)-16

A solution of alcohol (-)-15 (5.00 g, 11.4 mmol) in anhydrous pyridine (30 mL) was cooled to 0° C. and treated with TsCl (3.91 g, 20.5 mmol). After 30 min at 0° C. and 5 h at room temperature, the reaction was quenched with saturated aqueous NaHCO₃ (20 mL). The mixture was diluted with ether (200 mL), washed with aqueous NaHSO₄ (1.0 M), aqueous NaHCO₃ (10%), brine (200 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (10% ethyl acetate/hexane) provided (-)-15 (6.76 g, 100% yield) as white solid: mp 71-72° C.; [α]²³ _(D) -23.2° ©1.42, CHCl₃); IR (CHCl₃) 3020 (m), 3000 (m), 2960 (s), 2935 (s), 2880 (m), 2855 (s), 1617 (m), 1600 (m), 1590 (m), 1518 (m), 1495 (w), 1462 (s), 1390 (m), 1360 (s), 1302 (m), 1250 (s), 1190 (s), 1178 (s), 1120 (s), 1098 (s), 1085 (s), 1070 (s, 1032 (s), 963 (s), 900 (m), 830 (s), 810 (s), 653 (m); ¹ H NMR (500 MHZ, CDCl₃) d 7.70 (d, J=8.3 Hz, 2 H), 7.34 (d, J=8.7 Hz, 2 H), 7.25 (d, J=8.8 Hz, 2 H), 6.86 (d, J=8.7 Hz, 2 H), 5.36 (s, 3 H), 4.07 (dd, J=11.2, 4.7 Hz, 1 H), 3.85 (dd, J=7.3, 2.7 Hz, 1 H), 3.79 (s, 3 H), 3.71 (dd, J=7.1, 1.7 Hz, 1 H), 3.48 (dd, J=9.9, 1.4 Hz, 1 H), 3.45 (apparent t, J=11.1 Hz, 1 H), 2.40 (s, 3 H), 2.15 (dqd, J=13.9, 7.0, 1.7 Hz, 1 H), 2.05-1.96 (m, 1 H), 1.83 (dqd, J=7.1, 7.1, 1.6 Hz, 1 H), 0.94 (d, J=7.1 Hz, 3 H), 0.82 (s, 9 H), 0.81 (d, J=7.7 Hz, 3 H), 0.69 (d, J=6.7 Hz, 3 H), -0.04 (s, 3 H), -0.11 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.8, 144.6, 133.2, 131.3, 129.7, 127.9, 127.3, 113.5, 100.9, 82.0, 73.7, 73.2, 73.0, 55.2, 38.4, 35.5, 30.6, 26.0, 21.6, 18.3, 12.2, 10.6, 10.3, -3.9, -4.3; high resolution mass spectrum (FAB, NBA) m/z 593.2955 [(M+H)⁺ ; calcd for C₃₁ H₄₉ O₇ SSi: 593.2968].

EXAMPLE 10 Fragment (-)-A

From Tosylate (-)-16: A solution of Tosylate (-)-16 (6.76 g, 11.4 mmol) in anhydrous DMF (50 mL) was treated with NaI (17.1 g, 114.0 mmol), heated at 60° C. for 1.5 h, and cooled to room temperature. The mixture was diluted with ether (200 mL), washed with water (200 mL), saturated aqueous Na₂ S₂ O₃ (100 mL), brine (200 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (3% ethyl acetate/hexane) provided (-)-A (5.87 g, 94 % yield) as a colorless oil.

From Alcohol (-)-15: A solution of alcohol (-)-15 (4.70 g, 10.7 mmol), PPh₃ (4.21 g, 16.1 mmol) and imidazole (1.09 g, 16.1 mmol) in benzene/ether (1:2, 75 mL) was treated with I₂ (4.08 g, 16.1 mmol) under vigorous stirring. The mixture was stirred 1 h then diluted with ether (200 mL), washed with saturated Na₂ S₂ O₃, brine (100 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (2% ethyl acetate/hexane) furnished (-)-A (5.56 g, 95% yield) as a colorless oil: [α]²³ _(D) -39.3° ©2.01, CHCl₃); IR (CHCl₃) 3015 (m), 2960 (s), 2940 (s), 2860 (m), 1620 (w), 1520 (m), 1465 (m), 1430 (w), 1390 (m), 1305 (w), 1255 (s), 1230 (m), 1215 (m), 1205 (m), 1170 (m), 1120 (m), 1070 (m), 1035 (m), 990 (w), 970 (w), 930 (w), 830 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.39 (d, J=8.7 Hz, 2 H), 6.86 (d, J=8.8 Hz, 2 H), 5.40 (s, 1 H), 4.09 (dd, J=11.2, 4.7 Hz, 1 H), 3.85 (dd, J=7.1, 1.9 Hz, 1 H), 3.79 (s, 3 H), 3.48 (dd, J=8.2, 1.5 Hz, 1 H), 3.47 (apparent t, J=11.1 Hz, 1 H), 3.18-3.12 (m, 2 H), 2.11-2.00 (m, 2 H), 1.84 (ddq, J=7.1, 7.1, 1.6 Hz, 1 H), 1.02 (d, J=7.1 Hz, 3 H), 0.98 (d, J=6.7 Hz, 3 H), 0.89 (s, 9 H), 0.72 (d, J=6.7 Hz, 3 H), 0.06 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.8, 131.4, 127.4, 113.4, 100.9, 82.4, 75.5, 73.2, 55.3, 39.6, 38.7, 30.7, 26.2, 18.4, 14.7, 14.5, 12.2, 10.7, -3.7, -3.8; high resolution mass spectrum (CI, NH₃) m/z 548.1833 [(M)⁺ ; calcd for C₂₄ H₄₁ IO₄ Si: 548.1819].

Anal. Calcd for C₂₄ H₄₁ O₄ ISi: C, 52.55; H, 7.53. Found: C, 52.77; H, 7.68.

EXAMPLE 11 Amide (+)-17

A solution of common precursor (+)-5 (12.1 g, 37.2 mmol) and 2,6-lutidine (7.80 mL, 70.0 mmol) in CH₂ Cl₂ (90 mL) was cooled to 0° C. and tert-Butyldimethylsilyl trifluoromethanesulfonate (12.8 mL, 55.8 mmol) was added over 10 min. After 1.5 h, the mixture was diluted with Et₂ O (100 mL), washed with aqueous NaHSO₄ (1.0 M), brine (200 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (10% ethyl acetate/hexanes) provided (+)-17 (16.4 g, 100% yield) as a colorless oil: [α]²³ _(D) +9.49° ©1.47, CHCl₃); IR (CHCl₃) 3018 (s), 2970 (s), 2945 (s), 2900 (m), 2870 (s), 1658 (s),1620 (m), 1592 (w), 1520 (s), 1470 (s), 1448 (m), 1425 (m), 1393 (m), 1367 (m), 1308 (m), 1255 (s), 1213 (s), 1185 (m), 1178 (m), 1115 (s), 1084 (s), 1042 (s), 1000 (s), 940 (w), 928 (w), 871 (s), 839 (s), 770 (s), 726 (s), 664 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.21 (d, J=8.7 Hz, 2 H), 6.83 (d, J=8.7, 2 H), 4.36 (ABq, J_(AB) =11.6 Hz, Δδ_(AB) =17.3 Hz, 2 H), 3.92 (dd, J=8.2, 3.0 Hz, 1 H), 3.77 (s, 3 H), 3.55 (s, 3 H), 3.54 (dd, J=9.2, 2.5 Hz, 1 H), 3.13 (dd, J=9.2, 7.8 Hz, 1 H), 3.09 (s, 3 H), 3.15-3.09 (m, 1 H), 1.92-1.87 (m, 1 H), 1.09 (d, J=7.0 Hz, 3 H), 0.98 (d, J=7.0 Hz, 3 H), 0.88 (s, 9 H), 0.04 (apparent s, 6 H); ¹³ C NMR (125 MHZ, CDCl₃) d 176.8, 159.1, 130.9, 129.2, 113.7, 76.0, 72.7, 71.9, 61.1, 55.2, 39.3, 38.9, 26.1, 18.4, 15.3, 15.0, -3.87, -3.93; high resolution mass spectrum (CI, NH₃) m/z 440.2823 [(M+H)⁺ ; calcd for C₂₃ H₄₂ NO₅ Si: 440.2832].

Anal. Calcd for C₂₃ H₄₁ NO₅ Si: C, 62.83; H, 9.40. Found: C, 63.05; H, 9.32.

EXAMPLE 12 Aldehyde (+)-18

A solution of amide (+)-17 (9.19 g, 20.9 mmol) in THF (350 mL) was cooled to -78° C. and DIBAL (1.0 M in hexane, 44.0 mL, 44.0 mmol) was added over 30 min. After 0.5 h at -78° C., the reaction was quenched with MeOH (10 mL). The mixture was diluted with ether (500 mL), washed with saturated aqueous Rochelle's salt, brine (300 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (10% ethyl acetate/hexane) gave (+)-18 (7.05 g, 89% yield) as a colorless oil: [α]²³ _(D) +23.2° ©1.49, CHCl₃); IR (CHCl₃) 2960 (s), 2930 (s), 2860 (s), 1730 (s), 1610 (m), 1583 (w), 1510 (m), 1460 (m), 1373 (m), 1360 (w), 1300 (m), 1245 (s), 1170 (m), 1085 (m), 1033 (s), 933 (w), 835 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 9.67 (d, J=0.9 Hz, 1 H), 7.22 (d, J=8.7 Hz, 2 H), 6.86 (d, J=8.7 Hz, 2 H), 4.37 (ABq, J_(AB) =11.6 Hz, Δδ_(AB) =23.6 Hz, 2 H), 4.18 (dd, J=6.1, 3.7 Hz, 1 H), 3.78 (s, 3 H), 3.41 (dd, J=9.2, 5.7 Hz, 1 H), 3.31 (dd, J=9.2, 6.0 Hz, 1 H), 2.47 (qdd, J=7.1, 3.7, 0.9 Hz, 1 H), 2.03-1.95 (m, 1 H), 1.08 (d, J=7.0 Hz, 3 H), 0.94 (d, J=7.0 Hz, 3 H), 0.84 (s, 9 H), 0.04 (s, 3 H), -0.03 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 204.8, 159.2, 130.5, 129.2, 113.8, 72.7, 72.4, 71.7, 55.3, 50.0, 38.3, 25.9, 18.2, 14.3, 8.4, -4.1, -4.4; high resolution mass spectrum (FAB, NBA) m/z 403.2304 [(M+Na)⁺ ; calcd for C₂₁ H₃₆ O₄ SiNa: 403.2280].

EXAMPLE 13 Bromo Ester 19

A solution of aldehyde (+)-18 (822.1 mg, 2.16 mmol) in benzene (20 mL) was treated with Ph₃ P═CBrCO₂ Et (2.28 g, 5.34 mmol), heated at reflux for 40 h and cooled to room temperature. The mixture was filtered through a short silica column (20% ethyl acetate/hexane) and concentrated. Flash chromatography (3% ethyl acetate/hexane) afforded Z-Bromo ester (-)-19 (861.4 mg, 75% yield) and E-Bromo Ester (+)-19 (101.0 mg, 8.8% yield).

Z-Bromo Ester (-)-19: Colorless oil; [α]²³ _(D) -6.38° ©1.85, CHCl₃); IR (CHCl₃) 2960 (s), 2940 (s), 2860 (s), 1725 (s), 1618 (m), 1590 (w), 1515 (s), 1468 (m), 1390 (m), 1370 (m), 1303 (m), 1250 (s, br), 1176 (m), 1090 (s), 1037 (s), 1008 (m), 950 (m), 940 (m), 840 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, C₆ D₆) d 7.45 (d, J=9.7 Hz, 1 H), 7.26 (d, J=8.6 Hz, 2 H), 6.80 (d, J=8.7 Hz, 2 H), 4.37 (ABq, J_(AB) =11.6 Hz, Δδ_(AB) =19.3 Hz, 2 H), 3.99, (dq, J=10.8, 7.1 Hz, 1 H), 3.94 (dq, J=10.8, 7.1 Hz, 1 H), 3.82 (apparent t, J=5.4 Hz, 1 H), 3.41 (dd, J=9.1, 6.3 Hz, 1 H), 3.31 (s, 3 H), 3.30 (dd, J=9.2, 6.5 Hz, 1 H), 3.13-3.06 (m, 1 H), 2.05 (apparent septet, J=6.9 Hz, 1 H), 1.013 (d, J=7.0 Hz, 3 H), 1.006 (d, J=6.8 Hz, 3 H), 0.97 (s, 9 H), 0.92 (apparent t, J=7.1 Hz, 3 H), 0.06 (s, 3 H), 0.05 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 162.5, 159.1, 149.6, 130.8, 129.0, 114.9, 113.7, 75.5, 72.6, 72.2, 62.4, 55.3, 40.2, 38.9, 26.0, 18.3, 14.2, 14.1, 13.7, -4.0, -4.2; high resolution mass spectrum (CI, NH₃) m/z 546.2270 [(M+NH₄)⁺ ; calcd for C₂₅ H₄₅ NO₅ BrSi: 546.2251].

Anal. Calcd for C₂₅ H₄₁ O₅ BrSi: C, 56.70; H, 7.80. Found: C, 56.96; H, 7.86.

E-Bromo Ester (+)-19. Colorless oil; [α]²³ _(D) +3.2° ©1.65, CHCl₃); IR (CHCl₃) 2965 (s), 2940 (s), 2905 (m), 2890 (m), 2865 (s), 1720 (s), 1617 (m), 1590 (w), 1518 (s), 1468 (s), 1375 (s), 1350 (m), 1305 (m), 1250 (s, br), 1177 (m), 1090 (s), 1035 (s), 1007 (m), 950 (m), 840 (s), 675 (w) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.23 (d, J=8.6 Hz, 2 H), 6.86 (d, J=8.7 Hz, 2 H), 6.56 (d, J=10.6 Hz, 1 H), 4.39 (apparent s, 2 H), 4.24 (dq, J=10.8, 7.1 Hz, 1 H), 4.22 (dq, J=10.8, 7.1 Hz, 1 H), 3.79 (s, 3 H), 3.61 (dd, J=5.5, 5.0 Hz, 1 H), 3.43 (dd, J=9.2, 5.5 Hz, 1 H), 3.39-3.32 (m, 1 H), 3.24 (dd, J=9.1, 7.2 Hz, 1 H), 1.98-1.90 (m, 1 H), 1.30 (apparent t, J=7.1 Hz, 1 H), 1.00 (d, J=6.7 Hz, 3 H), 0.94 (d, J=7.0 Hz, 3 H), 0.89 (s, 9 H), 0.05 (s, 3 H), 0.03 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 162.8, 159.1, 151.9, 130.8, 129.1, 113.7, 110.2, 76.3, 72.6, 72.2, 62.1, 55.2, 38.8, 26.1, 18.3, 14.7, 14.1, 13.9, -4.06, -4.10; high resolution mass spectrum (CI, NH₃) m/z 529.1982 [(M+H)⁺ ; calcd for C₂₅ H₄₂ BrO₅ Si: 529.1985].

Anal. Calcd for C₂₅ H₄₁ O₅ BrSi: C, 56.70; H, 7.80. Found: C, 56.83; H, 7.99.

EXAMPLE 14 Allylic Alcohol (-)-20

A solution of ester (-)-19 (858.4 mg, 1.62 mmol) in CH₂ Cl₂ (16 mL) was cooled to -78° C. and DIBAL (1.0 M in hexane, 3.60 mL, 3.60 mmol) was added over 10 min. After 5 min at -78° C. and 10 min at room temperature, the reaction was quenched with MeOH (200 mL), followed by addition of saturated aqueous Rochelle's salt dropwise with stirring until a solid precipitated. The solution was separated by decanting (3×30 mL rinse, ethyl acetate) and the combined organic solutions were dried over MgSO₄, and concentrated. Flash chromatography (10% ethyl acetate/hexane) provided (-)-20 (674.5 mg, 85% yield) as a colorless oil: [α]²³ _(D) -15.5° ©2.51, CHCl₃); IR (CHCl₃) 3600 (w), 3420 (w, br), 3010 (m), 2960 (s), 2940 (s), 2890 (m), 2860 (s), 1618 (m), 1590 (w), 1520 (s), 1470 (m), 1380 (m), 1315 (m), 1307 (m), 1255 (s), 1178 (m), 1085 (s), 1039 (s), 1010 (m), 972 (m), 940 (m), 840 (s), 675 (m), 660 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.24 (d, J=8.7 Hz, 2 H), 6.87 (d, J=8.7 Hz, 2 H), 5.88 (br d, J=9.3 Hz, 1 H), 4.39 (ABq, J_(AB) =11.6 Hz, Δδ_(AB) =18.3 Hz, 2 H), 4.16 (apparent d, J=5.6 Hz, 2 H), 3.79 (s, 3 H), 3.59 (apparent t, J=5.3 Hz, 1 H), 3.48 (dd, J=9.2, 5.3 Hz, 1 H), 3.23 (dd, J=9.2, 7.7 Hz, 1 H), 2.82-2.76 (m, 1 H), 2.00-1.92 (m, 1 H), 0.98 (d, J=6.9 Hz, 3 H), 0.97 (d, J=6.8 Hz, 3 H), 0.88 (s, 9 H), 0.024 (s, 3 H), 0.016 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.1, 134.1, 130.9, 129.1, 125.1, 113.7, 76.5, 72.6, 72.3, 68.4, 55.3, 39.1, 38.7, 26.1, 18.4, 14.9, 14.3, -3.9, -4.0; high resolution mass spectrum (CI, NH₃) m/z 487.1873 [(M+H)⁺ ; calcd for C₂₃ H₄₀ O₄ BrSi: 487.1879].

Anal. Calcd for C₂₃ H₃₉ O₄ BrSi: C, 56.66; H, 8.06. Found: C, 56.72; H, 8.07.

EXAMPLE 15 Mesylate (-)-21

A solution of alcohol (-)-20 (6.85 g, 14.1 mmol) in CH₂ Cl₂ (150 mL) was cooled to 0° C. and MsCl (2.20 mL, 28.4 mmol) was added over 2 min. After 10 min, the reaction was quenched with aqueous NaHSO₄ (1.0 M, 100 mL). The organic phase was washed with water (100 mL), dried over MgSO₄, and concentrated. Flash chromatography (10% ethyl acetate/hexane) afforded (-)-21 (7.85 g, 99% yield) as a colorless oil: [α]²³ _(D) -14.6° ©1.40, CHCl₃); IR (CHCl₃) 3020 (m), 2960 (s), 2940 (s), 2880 (m), 2860 (s), 1730 (w), 1610 (m), 1583 (m), 1510 (s), 1460 (m), 1410 (m), 1362 (s), 1300 (m), 1250 (s), 1220 (s), 1175 (s), 1080 (s), 1032 (s), 1002 (m), 960 (m), 937 (s), 835 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.23 (d, J=8.6 Hz, 2 H), 6.86 (d, J=8.6 Hz, 2 H), 6.07 (d, J=9.4 Hz, 1 H), 4.74 (d, J=0.4 Hz, 2 H), 4.38 (ABq, J_(AB) =11.7 Hz, Δδ_(AB) =25.5 Hz, 2 H), 3.79 (s, 3 H), 3.61 (apparent t, J=5.2 Hz, 1 H), 3.44 (dd, J=9.2, 5.7 Hz, 1 H), 3.22 (dd, J=9.2, 7.3 Hz, 1 H), 3.01 (s, 3 H), 2.84-2.77 (m, 1 H), 1.99-1.91 (m, 1 H), 0.98 (d, J=6.8 Hz, 3 H), 0.96 (d, J=7.0 Hz, 3 H), 0.88 (s, 9 H), 0.03 (s, 3 H), 0.02 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.1, 140.9, 130.8, 129.1, 116.7, 113.8, 76.1, 74.2, 72.6, 72.1, 55.3, 39.6, 38.8, 38.5, 26.0, 18.3, 14.7, 14.3, -3.9, -4.0; high resolution mass spectrum (CI, NH₃) m/z 582.1911 [(M+NH₄)⁺ ; calcd for C₂₄ H₄₅ NO₆ BrSSi: 582.1920].

EXAMPLE 16 Vinyl Bromide (-)-22

A solution of mesylate (-)-21 (6.43 g, 11.4 mmol) in benzene (120 mL) was treated with LiBHEt₃ (1.0 M in THF, 25.0 mL, 25.0 mmol) at room temperature. After 0.5 h, the reaction was quenched with aqueous NaOH (1.0 N, 50 mL). The mixture was diluted with ethyl acetate (200 mL), washed with brine (2×200 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (5% ethyl acetate/hexane) provided (-)-22 (4.86 g, 91%) as a colorless oil: [α]²³ _(D) -16.9° ©1.69, CHCl₃); IR (CHCl₃) 3005 (m), 2965 (s), 2935 (s), 2860 (s), 1660 (w), 1610 (m), 1585 (w), 1510 (m), 1460 (m), 1425 (w), 1377 (m), 1360 (m), 1300 (m), 1250 (s), 1180 (m), 1170 (m), 1075 (s), 1030 (m), 860 (m), 835 (s), 805 (m), 660 (w) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.24 (d, J=8.6 Hz, 2 H), 6.86 (d, J=8.6 Hz, 2 H), 5.47 (apparent dd, J=9.0, 1.2 Hz, 1 H), 4.39 (ABq, J_(AB) =11.7 Hz, Δδ_(AB) =15.8 Hz, 2 H), 3.79 (s, 3 H), 3.56 (apparent t, J=5.4 Hz, 1 H), 3.50 (dd, J=9.1, 5.1 Hz, 1 H), 3.22 (dd, J=8.8, 8.1 Hz, 1 H), 2.74-2.67 (m, 1 H), 2.21 (d, J=1.1 Hz, 3 H), 1.99-1.91 (m, 1 H), 0.98 (d, J=6.9 Hz, 3 H), 0.94 (d, J=6.8 Hz, 3 H), 0.88 (s, 9 H), 0.01 (s, 3 H), 0.00 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.1, 133.4, 131.0, 129.1, 120.6, 113.7, 76.7, 72.6, 72.5, 55.3, 39.7, 38.7, 28.8, 26.1, 18.4, 14.8, 14.4, -3.96, -4.01; high resolution mass spectrum (FAB, NBA) m/z 493.1763 [(M+Na)⁺ ; calcd for C₂₃ H₃₉ O₃ BrSiNa: 493.1750].

EXAMPLE 17 Vinyl Silane (-)-23

A solution of vinyl bromide (-)-22 (83.2 mg, 0.177 mmol) in THF (2.0 mL) was cooled to -78° C. and n-BuLi (1.6 M in hexane, 260 ml, 416 mmol) was added over 10 min. After 1 h at -78° C. and 15 min at room temperature, the reaction was quenched with H₂ O (200 mL). The mixture was concentrated and dissolved in ethyl acetate (30 mL), washed with water (30 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (5% ethyl acetate/hexane) provided (-)-23 (47.9 mg, 69% yield) as a colorless oil: [α]²³ _(D) -61.5° ©0.615, CHCl₃); IR (CHCl₃) 3680 (w), 3470 (m, br), 1614 (m), 1588 (w), 1513 (s), 1465 (m), 1442 (m), 1415 (m), 1360 (m), 1302 (m), 1250 (s), 1176 (m), 1120 (m), 1077 (m), 1032 (m), 992 (m), 830 (s), 820 (s), 805 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.22 (d, J=8.7 Hz, 2 H), 6.85 (d, J=8.7 Hz, 2 H), 6.22 (dq, J=10.5, 1.6 Hz, 1 H), 4.42 (ABq, J_(AB) =11.4 Hz, Δδ_(AB) =18.8 Hz, 2 H), 3.78 (s, 3 H), 3.65 (br s, 1 H), 3.56 (dd, J=9.1, 4.0 Hz, 1 H), 3.44 (dd, J=8.8, 2.9 Hz, 1 H), 3.42 (apparent t, J=8.8 Hz, 1 H), 2.45 (dqd, J=10.3, 6.6, 2.7 Hz, 1 H), 1.95-1.87 (m, 1 H), 1.78 (d, J=1.6 Hz, 3 H), 0.91 (d, J=6.7 Hz, 3 H), 0.87 (s, 9 H), 0.80 (d, J=7.0 Hz, 3 H), 0.09 (s, 3 H), 0.08 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.4, 147.7, 130.8, 129.7, 129.4, 113.9, 79.9, 76.4, 73.3, 55.3, 38.1, 36.3, 27.1, 26.6, 17.8, 13.4, 13.1, -3.4, -3.7; high resolution mass spectrum (CI, NH₃) m/z 393.2821 [(M+H)⁺ ; calcd for C₂₃ H₄₁ O₃ Si: 393.2824].

Anal. Calcd for C₂₃ H₄₀ O₃ Si: C, 70.36; H, 10.27. Found: C, 70.58; H, 10.57.

EXAMPLE 18 trans Olefin (+)-24

A solution of vinyl bromide (-)-22 (27.8 mg, 0.0591 mmol) in ether (600 μL) was cooled to -78° C., and t-BuLi (1.7 M in pentane, 103 μL, 0.175 mmol) was added over 2 min. After 10 min at -78° C. and 5 min at room temperature, the reaction was quenched with MeOH (100 mL). The mixture was filtered through a short silica plug, and concentrated. Flash chromatography (1% ethyl acetate/hexane) provided (+)-24 (21.9 mg, 94% yield) as a colorless oil; [α]²³ _(D) +19.3° ©1.10, CHCl₃); IR (CHCl₃) 3000 (m), 2960 (s), 2935 (s), 2880 (m), 2860 (s), 1612 (m), 1587 (w), 1510 (s), 1462 (m), 1440 (m), 1405 (w), 1375 (m), 1360 (m), 1300 (m), 1250 (s), 1170 (m), 1090 (s), 1034 (s), 1002 (m), 970 (m), 934 (w), 850 (m), 832 (s), 720 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, C₆ D₆) d 7.24 (d, J=8.7 Hz, 2 H), 6.80 (d, J=8.6 Hz, 2 H), 5.43 (ddq, J=15.3, 7.8, 1.4 Hz, 1 H), 5.34 (dqd, J=15.4, 6.3, 0.7 Hz, 1 H), 4.38 (ABq, J_(AB) =11.7 Hz, Δδ_(AB) =30.7 Hz, 2 H), 3.58 (apparent t, J=5.2 Hz, 1 H), 3.57 (dd, J=9.0, 5.1 Hz, 1 H), 3.36 (dd, J=9.0, 7.2 Hz, 1 H), 3.30 (s, 3 H), 2.39 (ddq, J=6.8, 6.8, 6.8 Hz, 1 H), 2.17-2.10 (m, 1 H), 1.58 (apparent d, J=6.1 Hz, 3 H), 1.07 (d, J=7.2 Hz, 3 H), 1.05 (d, J=6.9 Hz, 3 H), 1.00 (s, 9 H), 0.10 (s, 3 H), 0.08 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.0, 135.6, 131.1, 129.1, 123.9, 113.7, 78.4, 72.6, 72.5, 55.3, 40.4, 37.9, 26.2, 26.1, 18.4, 18.0, 15.9, 15.1, -3.8, -4.1; high resolution mass spectrum (CI, NH₃) m/z 393.2836 [(M+H)⁺ ; calcd for C₂₃ H₄₁ O₃ Si: 393.2824].

EXAMPLE 19 Alcohol (-)-25

A solution of PMB ether (-)-22 (50.0 mg, 0.106 mmol) and PMB acetal (-)-15 (46.5 mg, 0.106 mmol) in CH₂ Cl₂ (2.0 mL) was cooled to 0° C., then treated with H₂ O (100 mL) and DDQ (26.5 mg, 0.117 mmol). After 30 min, the mixture was diluted with ether (60 mL), washed with saturated aqueous NaHCO₃ (60 mL), brine (3×60 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (gradient elution, 5%->10% ethyl acetate/hexane) afforded (-)-25 (31.0 mg, 83% yield) and recovered (-)-15 (40.0 mg, 86% recovery).

(-)-25: [α]²³ _(D) -13.3° ©0.99, CHCl₃); IR (CHCl₃) 3640 (w), 3520 (m), 3000 (m), 2960 (s), 2940 (s), 2890 (m), 2860 (s), 1660 (w), 1472 (m), 1465 (m), 1440 (m), 1407 (m), 1390 (m), 1380 (m), 1360 (m), 1258 (s), 1072 (s), 1023 (s), 1005 (s), 980 (m), 937 (m), 847 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 5.50 (apparent dd, J=9.0, 1.1 Hz, 1 H), 3.65 (dd, J=11.0, 4.8 Hz, 1 H), 3.59 (dd, J=11.0, 5.7 Hz, 1 H), 3.56 (apparent t, J=5.2 Hz, 1 H), 2.80-2.72 (m,l H), 2.25 (d, J=1.0 Hz, 3 H), 2.20 (br s, 1 H), 1.86-1.78 (m, 1 H), 0.99 (d, J=7.1 Hz, 3 H), 0.98 (d, J=6.9 Hz, 3 H), 0.90 (s, 9 H), 0.09 (s, 3 H), 0.05 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 132.6, 121.7, 79.7, 65.6, 40.9, 38.8, 28.9, 26.1, 18.3, 15.5, 15.0, -3.9, -4.0; high resolution mass spectrum (CI, NH₃) m/z 351.1087 [M⁺ ; calcd for C₁₅ H₃₁ O₂ BrSi: 351.1093].

EXAMPLE 20 Alcohol (+)-26

A solution of amide (+)-17 (323.5 mg, 0.738 mmol) in EtOH (8.0 mL) was stirred for 5 h under H₂ atmosphere in the presence of Pearlman's catalyst (20% Pd(OH)₂ /C, 104.1 mg), then filtered and concentrated. Flash chromatography (10 mL silica, 20% ethyl acetate/hexane) provided (+)-26 (216.7 mg, 92% yield) as a colorless oil: [α]²³ _(D) +16.1° ©2.60, CHCl₃); IR (CHCl₃) 3480 (m, br), 3000 (s), 2958 (s), 2935 (s), 2880 (s), 2860 (s), 1635 (s), 1460 (s), 1415 (m), 1390 (s), 1360 (m) 1285 (w), 1255 (s), 1174 (m), 1148 (m), 1093 (s), 1070 (s), 1047 (s), 1033 (s), 990 (s), 935 (m), 905 (w), 860 (s), 830 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 4.05 (dd, J=9.1, 3.1 Hz, 1 H), 3.69 (s, 3 H), 3.55-3.50 (m, 1 H), 3.23 (ddd, J=10.1, 10.1, 2.8 Hz, 1 H), 3.13 (s, 3 H), 3.09 (br m, 1 H), 2.81 (br m, 1 H), 1.91-1.83 (m, 1 H), 1.14 (d, J=7.0 Hz, 3 H), 0.879 (d, J=7.0 Hz, 3 H), 0.879 (s, 9 H), 0.08 (s, 3 H), 0.06 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 177.3, 75.2, 64.9, 61.5, 40.8, 38.2, 32.2, 26.0, 18.2, 15.9, 12.8, -4.1, -4.3; high resolution mass spectrum (CI, NH₃) m/z 320.2265 [(M+H)⁺ ; calcd for C₁₅ H₃₄ NO₄ Si: 320.2256].

EXAMPLE 21 Aldehyde (+)-27

A solution of alcohol (+)-26 (8.80 g, 27.5 mmol) and NEt₃ (15.3 mL, 110 mmol) in CH₂ Cl₂ (50 mL) was cooled to -10° C. and treated with SO₃.pyr (13.1 g, 82.6 mmol) in DMSO (100 mL). After 20 min at room temperature, the mixture was diluted with ether (300 mL), washed with aqueous NaHSO₄ (1.0 M, 200 mL), brine (4×200 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (20% ethyl acetate/hexane) afforded (+)-27 (8.55 g, 98% yield) as a colorless oil: [α]²³ _(D) +51.2° ©1.00, CHCl₃); IR (CHCl₃) 3010 (m), 2960 (s), 2940 (s), 2895 (m), 2865 (m), 1750 (m), 1720 (s), 1647 (s), 1460 (s), 1420 (m), 1390 (s), 1360 (m), 1255 (s), 1180 (m), 1105 (m), 1077 (m), 1040 (s), 995 (s), 936 (m), 853 (s), 837 (s), 710 (m), 657 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 9.68 (d, J=1.6 Hz, 1 H), 4.22 (dd, J=8.9, 2.6 Hz, 1 H), 3.68 (s, 3 H), 3.10 (apparent s, 4 H), 2.46 (qdd, J=7.1, 2.6, 1.5 Hz, 1 H), 1.16 (d, J=6.9 Hz, 3 H), 1.10 (d, J=7.0 Hz, 3 H), 0.88 (s, 9 H), 0.092 (s, 3 H), 0.088 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 203.2, 175.6, 75.1, 61.5, 52.1, 39.6, 32.1, 25.9, 18.2, 15.4, 10.2, -4.07, -4.11; high resolution mass spectrum (CI,NH₃) m/z 318.2096 [(M+H)⁺ ; C₁₅ H₃₂ NO₄ Si: 318.2100].

EXAMPLE 22 Dithiane (+)-28.

A solution of ZnCl₂ (dried at 140° C. for 1 h under vacuum, 170.5 mg, 1.25 mmol) in ether (6.0 mL) was cooled to 0° C. and (TMSSCH₂)₂ CH₂ (175.0 μL, 0.628 mmol) was added. The resultant white milky suspension was treated with aldehyde (+)-27 (180.0 mg, 0.567 mmol) in ether (6.0 mL). The mixture was stirred for 4.5 h at 0° C. and 1.5 h at room temperature, then partitioned between ethyl acetate (50 mL) and aqueous ammonia (30 mL). The organic phase was washed with brine (2×30 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (10% ethyl acetate/hexane) provided (+)-28 (182.9 mg, 79% yield) as a white solid: mp 55-57° C.; [α]²³ _(D) +18.5° ©1.44, CHCl₃); IR (CHCl₃) 3015 (m), 2970 (s), 2945 (s), 2910 (m), 2870 (m), 1665 (s), 1475 (m), 1470 (m), 1437 (m), 1430 (m), 1420 (m), 1390 (m), 1365 (m), 1320 (w), 1280 (m), 1260 (m), 1120 (m), 1115 (m), 1097 (m), 1080 (m), 1065 (m), 1040 (m), 1000 (m), 940 (w), 925 (w), 910 (w), 877 (m), 838 (s), 815 (m), 800 (m), 700 (w), 675 (w), 660 (w) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 4.33 (d, J=4.2 Hz, 1 H), 4.23 (dd, J=7.1, 3.6 Hz, 1 H), 3.68 (s, 3 H), 3.15 (s, 3 H), 2.98 (dq, J=6.8, 3.7 Hz, 1 H), 2.90 (ddd, J=14.1, 12.2, 2.5 Hz, 1 H), 2.83-2.77 (m, 3 H), 2.09-2.03 (m, 1 H), 1.94 (ddq, J=7.2, 7.2, 4.3 Hz, 1 H), 1.88-1.76 (m, 1 H), 1.08 (d, J=7.2 Hz, 3 H), 1.07 (d, J=6.9 Hz, 3 H), 0.90 (s, 9 H), 0.13 (s, 3 H), 0.02 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 176.2, 73.2, 61.0, 50.8, 44.2, 38.6, 31.3, 30.3, 26.2, 18.4, 12.9, 11.0, -4.1, -4.2; high resolution mass spectrum (CI, NH₃) m/z 408.2081 [(M+H)⁺ ; calcd for C₁₈ H₃₈ NO₃ S₂ Si: 408.2062].

Anal. Calcd. for C₁₈ H₃₇ NO₃ S₂ Si: C, 53.03; H, 9.15. Found: C, 53.06; H, 9.31.

EXAMPLE 23 Aldehyde (+)-29

A solution of dithiane (+)-28 (1.05 g, 2.58 mmol) in THF (40 mL) was cooled to -78° C. and DIBAL (1.0 M in hexane, 5.15 mL, 5.15 mmol) was added over 15 min. After 10 min at -78° C., the mixture was quenched with MeOH (2.0 mL) and partitioned between ether and saturated aqueous Rochelle's salt (50 mL each). The organic phase was washed with brine (30 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (10% ethyl acetate/hexane) provided (+)-29 (822 mg, 91% yield) as white solid: mp 54-55° C.; [α]²³ _(D) +50.8° ©1.19, CHCl₃); IR (CHCl₃) 2965 (s), 2940 (s), 2910 (s), 2865 (s), 2720 (w), 1730 (s), 1475 (m), 1467 (m), 1428 (m), 1418 (m), 1390 (m), 1365 (m), 1280 (m), 1260 (s), 1190 (m), 1150 (m), 1104 (s), 1070 (m), 1030 (s), 1007 (m), 953 (m), 940 (m), 910 (m), 835 (s), 810 (m), 675 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 9.70 (s, 1 H), 4.44 (dd, J=8.3, 2.2 Hz, 1 H), 4.38 (d, J=3.7 Hz, 1 H), 2.93 (ddd, J=14.1, 12.3, 2.6 Hz, 1 H), 2.84-2.80 (m, 3 H), 2.43 (qd, J=7.1, 2.2 Hz, 1 H), 2.13-2.07 (m, 1 H), 2.02 (dqd, J=8.2, 7.1, 3.7 Hz, 1 H), 1. 88-1.79 (m, 1 H), 1.10 (d, J=6.9 Hz, 3 H), 1.05 (d, J=7.1 Hz, 3 H), 0.87 (s, 9 H), 0.16 (s, 3 H), -0.01 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 204.6, 71.1, 51.0, 49.7, 43.5, 31.3, 30.3, 26.2, 26.0, 18.4, 12.9, 6.8, -3.9, -4.3; high resolution mass spectrum (CI, NH₃) m/z 349.1678 [(M+H)⁺ ; calcd for C₁₆ H₃₃ O₂ S₂ Si: 349.1691].

Anal. Calcd for C₁₆ H₃₂ O₂ S₂ Si: C,55.12; H, 9.25. Found: C, 55.08; H, 9.28.

EXAMPLE 24 Dimethoxy Acetal (+)-30

A solution of aldehyde (+)-29 (792 mg, 2.27 mmol) in HC(OMe)₃ /MeOH (48 mL, 1:5) was treated with TsOH•H₂ O (8.6 mg, 0.045 mmol) at room temperature. After 30 min, NEt₃ (1.0 mL) was added and the mixture was concentrated. Flash chromatography (10% ethyl acetate/hexane) provided (+)-30 (886 mg, 99% yield) as a white solid: mp 58-59° C.; [α]²³ _(D) +27.1° ©2.85, CHCl₃); IR (CHCl₃) 2960 (s), 2940 (s), 2905 (s), 2860 (m), 2835 (m), 1473 (m), 1463 (m), 1432 (m), 1425 (m), 1415 (m), 1387 (m), 1362 (m), 1340 (w), 1278 (m), 1252 (s), 1190 (m), 1158 (m), 1104 (s), 1070 (m), 1050 (m), 1030 (s), 1005 (m), 963 (m), 938 (m), 908 (m), 873 (m), 834 (s), 810 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 4.41 (d, J=3.1 Hz, 1 H), 4.23 (d, J=8.6 Hz, 1 H), 4.02 (dd, J=8.6, 1.3 Hz, 1 H), 3.29 (s, 3 H), 3.26 (s, 3 H), 2.93 (ddd, J=14.0, 12.4, 2.5 Hz, 1 H), 2.85-2.78 (m, 3 H), 2.11-2.05 (m, 1 H), 1.93-1.77 (m, 3 H), 1.00 (d, J=7.2 Hz, 3 H), 0.91 (s, 9 H), 0.85 (d, J=6.9 Hz, 3 H), 0.17 (s, 3 H), 0.09 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 105.0, 71.5, 53.0, 51.5, 51.2, 43.8, 37.4, 31.3, 30.2, 26.3, 18.8, 12.9, 8.1, -3.8, -4.3; high resolution mass spectrum (FAB, NBA) m/z 417.1934 [(M+Na)⁺ ; calcd for C₁₈ H₃₈ O₃ S₂ SiNa: 417.1930].

Anal. Calcd for C₁₈ H₃₈ O₃ S₂ Si: C, 54.78; H, 9.70. Found: C, 54.80; H, 9.66.

EXAMPLE 25 Hydroxy Acetal (-)-32

A solution of dithiane (+)-30 (3.60 g, 9.12 mmol) in 10% HMPA/THF (60 mL) was cooled to -78° C. and treated with t-BuLi (1.7 M in pentane, 5.63 mL, 9.58 mmol) dropwise over 15 min. The mixture was stirred 1 h at -78° C. and 1 h at -42° C., then recooled to -78° C. A solution of benzyl R-(-)-glycidyl ether (1.65 g, 10.0 mmol) in 10% HMPA/THF (12 mL) was added via cannula. After 0.5 h, the reaction mixture was warmed to -42° C. for 0.5 h and quenched with saturated aqueous NH₄ Cl (20 mL). The mixture was diluted with ether (200 mL), washed with water, brine (200 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (10% ethyl acetate/hexane) afforded (-)-32 (4.04 g, 79% yield) as a colorless oil: [α]²³ _(D) -5.9° ©2.1, CHCl₃); IR (CHCl₃) 3450 (w, br), 3020 (m), 2960 (s), 2940 (s), 2910 (m), 2860 (m), 2840 (m), 1605 (w), 1500 (w), 1475 (m), 1468 (m), 1458 (m), 1440 (m), 1430 (m), 1393 (m), 1387 (m), 1365 (m), 1280 (w), 1255 (m), 1233 (m), 1203 (m), 1167 (w), 1153 (w), 1110 (s), 1060 (m), 1045 (m), 1030 (m), 1010 (m), 980 (w), 940 (m), 910 (w), 860 (m), 837 (s), 800 (m), 695 (m), 670 (m), 660 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.35-7.25 (m, 5 H), 4.64 (dd, J=4.0, 1.1 Hz, 1 H), 4.57 (ABq, J_(AB) =12.1 Hz, Δδ_(AB) =17.8 Hz, 2 H), 4.21 (d, J=7.7 Hz, 1 H), 4.14-4.09 (m, 1 H), 3.48 (dd, J=9.5, 6.0 Hz, 1 H), 3.47 (dd, J=9.6, 5.0 Hz, 1 H), 3.37 (d, J=0.7 Hz, 1 H), 3.36 (s, 3 H), 3.29 (s, 3 H), 3.08 (ddd, J=14.4, 11.4, 2.9 Hz, 1 H), 2.95 (ddd, J=14.4, 11.3, 3.1 Hz, 1 H), 2.71-2.64 (m, 2 H), 2.59 (dqd, J=6.7, 6.7, 0.9 Hz, 1 H), 2.49 (dd, J=15.6, 7.9 Hz, 1 H), 2.30 (dq, J=4.0, 7.3 Hz, 1 H), 2.27 (dd, J=15.6, 2.3 Hz, 1 H), 2.04-2.00 (m, 1 H), 1.86-1.78 (m, 1 H), 1.18 (d, J=7.4 Hz, 3 H), 0.94 (d, J=6.8 Hz, 3 H), 0.90 (s, 9 H), 0.08 (s, 3 H), 0.07 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 138.2, 128.4, 127.6, 106.9, 74.4, 73.3, 70.0, 67.9, 55.7, 53.6, 52.6, 47.2, 39.4, 38.5, 26.3, 26.1, 26.0, 25.0, 18.3, 9.8, 9.5, -3.9, -4.9; high resolution mass spectrum (FAB, NBA) m/z 581.2763 [(M+Na)⁺ ; calcd for C₂₈ H₅₀ O₅ S₂ SiNa: 581.2767].

EXAMPLE 26 Ketone (+)-33

A solution of hydroxy acetal (-)-32 (3.94 g, 7.05 mmol) in H₂ O/MeOH (1:9, 75 mL) was treated with (CF₃ CO₂)₂ IPh (4.55 g, 10.6 mmol) at 0° C. After 5 min, the mixture was quenched with saturated NaHCO₃ (20 mL) and extracted with ether (200 mL). The organic phase was washed with brine (200 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (20% ethyl acetate/hexane) furnished (+)-33 (2.66 g, 80% yield) as a colorless oil. [α]²³ _(D) +36° ©0.36, CHCl₃); IR (CHCl₃) 3580 (w, br), 3005 (m), 2960 (s), 2930 (s), 2900 (m), 2860 (m), 1710 (m), 1463 (m), 1455 (m), 1387 (m), 1362 (m), 1253 (m), 1220 (m), 1105 (s), 1070 (s),1053 (s), 1030 (s), 1002 (m), 938 (m), 866 (m), 830 (s), 808 (m), 690 (m), 660 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.34-7.25 (m, 5 H), 4.54 (apparent s, 2 H), 4.40-4.25 (m, 1 H), 4.23 (dd, J=7.6, 1.9 Hz, 1 H), 4.19 (d, J=8.0 Hz, 1 H), 3.46 (dd, J=9.7, 4.9 Hz, 1 H), 3.43 (dd, J=9.7, 5.9 Hz, 1 H), 3.27 (s, 3 H), 3.25 (s, 3 H), 3.01 (d, J=3.8 Hz, 1 H), 2.76 (dd, J=18.0, 8.7 Hz, 1 H), 2.74 (dq, J=7.1, 7.1 Hz, 1 H), 2.62 (dd, J=17.9, 3.2 Hz, 1 H), 1.83 (dqd, J=8.0, 7.0, 1.9 Hz, 1 H), 0.97 (d, J=7.1 Hz, 3 H), 0.88 (d, J=6.9 Hz, 3 H), 0.83 (s, 9 H), 0.06 (s, 3 H), -0.05 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 213.0, 138.0, 128.4, 127.71, 127.68, 105.0, 73.4, 73.3, 71.8, 66.5, 52.9, 52.6, 52.3, 46.5, 37.9, 26.1, 18.4, 12.7, 8.8, -4.1, -4.8; high resolution mass spectrum (FAB, NBA) m/z 491.2821 [(M+Na)⁺ ; calcd for C₂₅ H₄₄ O₆ SiNa: 491.2805].

EXAMPLE 27 Diol (-)-34

A solution of Me₄ NBH(OAc)₃ (1.80 g, 6.84 mmol) in HOAc/CH₃ CN (1:1, 10.0 mL) was cooled to -40° C. and ketone (+)-33 (536 mg, 1.14 mmol) in CH₃ CN (5 mL) was added. After 12 h at -20° C., the mixture was treated with saturated aqueous Rochelle's salt (20 mL) and extracted with CH₂ Cl₂ (3×50 mL). The combined organic extracts were washed with saturated NaHCO₃, brine (100 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (1:1:1, CH₂ Cl₂ /ether/hexane) provided (-)-34 (519 mg, 97% yield) as a colorless oil: [α]²³ _(D) -7.78° ©0.900, CHCl₃); IR (CHCl₃) 3680 (w), 3460 (m, br), 3015 (m), 2960 (s), 2940 (s), 2900 (m), 2865 (s), 1470 (m), 1460 (m), 1390 (m), 1365 (m), 1260 (m), 1230 (m), 1208 (m), 1112 (s), 1065 (s), 1030 (m), 1010 (m), 942 (m), 865 (m), 838 (m), 698 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.33-7.30 (m, 4 H), 7.29-7.25 (m, 1 H), 4.55 (ABq, J_(AB) =12.0 Hz, Δδ_(AB) =15.7 Hz, 2 H), 4.16-4.11 (m, 1 H), 4.13 (d, J=7.8 Hz, 1 H), 4.07 (dd, J=4.8, 1.6 Hz, 1 H), 3.73 (br s, 1 H), 3.68 (dddd, J=9.3, 9.3, 2.4, 2.4 Hz, 1H), 3.50 (dd, J=9.6, 4.5 Hz, 1 H), 3.42 (dd, J=9.4, 7.0 Hz, 1 H), 3.38 (s, 3 H), 3.29 (s, 3 H), 3.09 (d, J=4.0 Hz, 1 H), 1.90 (dqd, J=7.0, 7.0, 1.5 Hz, 1 H), 1.76 (br dd, J=13.6, 8.5 Hz, 1 H), 1.68 (dqd, J=9.6, 6.9, 5.0 Hz, 1 H), 1.49 (ddd, J=14.3, 9.0, 2.9 Hz, 1 H), 0.894 (d, J=7.9 Hz, 3 H), 0.886 (s, 9 H), 0.80 (d, J=7.0 Hz, 3 H), 0.055 (s, 3 H), 0.048 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 138.2, 128.4, 127.7, 127.6, 107.3, 74.5, 73.3, 71.0, 70.9, 67.8, 55.2, 52.1, 45.9, 37.3, 36.9, 25.9, 18.2, 11.6, 10.6, -4.3, -4.7; high resolution mass spectrum (FAB, NBA) m/z 493.2951 [(M+Na)⁺ ; calcd for C₂₅ H₄₆ O₆ SiNa: 493.2962].

EXAMPLE 28 Alcohol (-)-35

A solution of (-)-34 (123.3 mg, 0.262 mmol) in benzene (10 mL) was treated with TsOH•H₂ O (2.0 mg, 0.0105 mmol) at room temperature. After 20 min, the mixture was quenched with NEt₃ (1.0 mL) and concentrated. Flash chromatography (2% ether/CH₂ Cl₂) afforded 35 (100.1 mg, β/α=2:1, 87% yield) as a colorless oil.

β Anomer (35): [α]²³ _(D) -3.3° ©2.25, CHCl₃); IR (CHCl₃) 3680 (w), 3580 (w), 3490 (w), 3010 (m), 2960 (s), 2930 (s), 2880 (m), 2860 (s), 1603 (w), 1525 (w), 1515 (w), 1493 (m), 1470 (m), 1460 (m), 1450 (m), 1387 (m), 1360 (m), 1347 (m), 1330 (m), 1253 (s), 1225 (m), 1200 (m), 1143 (m), 1110 (s), 1070 (s), 1045 (s), 1020 (s), 1015 (m), 1003 (m), 985 (m), 950 (m), 870 (m), 853 (m), 833 (s), 807 (m), 800 (m), 790 (m), 690 (m), 670 (m), 657 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.34-7.25 (m, 5 H), 4.69 (d, J=2.4 Hz, 1 H), 4.55 (ABq, J_(AB) =12.0 Hz, Δδ_(AB) =14.6 Hz, 2 H), 4.17-4.12 (m, 1 H), 3.78 (ddd, J=9.7, 9.7, 2.5 Hz, 1 H), 3.60 (apparent t, J=2.7 Hz, 1 H), 3.51 (dd, J=9.5, 4.1 Hz, 1 H), 3.42 (s, 3 H), 3.39 (dd, J=9.5, 7.0 Hz, 1 H), 2.86 (d, J=3.8 Hz, 1 H), 1.88 (apparent qt, J=7.1, 2.7 Hz, 1 H), 1.76 (ddd, J=14.4, 8.9, 2.6 Hz, 1 H), 1.72-1.65 (m, 1 H), 1.53 (ddd, J=14.4, 9.3, 2.9 Hz, 1 H), 0.90 (d, J=8.2 Hz, 3 H), 0.89 (s, 9 H), 0.78 (d, J=6.8 Hz, 3 H), 0.04 (s, 3 H), 0.02 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 138.2, 128.4, 127.7, 101.2, 76.7, 74.7, 73.3, 73.0, 67.4, 56.6, 41.1, 36.0, 34.7, 25.9, 18.1, 13.7, 9.7, -4.6, -4.9; high resolution mass spectrum (FAB, NBA) m/z 461.2693 [(M+Na)⁺ ; calcd for C₂₄ H₄₂ O₅ SiNa: 461.2699].

α Anomer (35): [α]²³ _(D) +48° ©0.54, CHCl₃); IR (CHCl₃) 3670 (w), 3570 (w), 3480 (w, br), 3005 (m), 2960 (s), 2930 (s), 2880 (m), 2855 (s), 1600 (w), 1527 (w), 1515 (w), 1495 (w), 1460 (m), 1360 (m), 1253 (s), 1225 (m), 1212 (m), 1200 (m), 1170 (m), 1148 (m), 1106 (s), 1087 (s), 1048 (s), 1030 (s), 963 (m), 872 (m), 833 (s), 788 (m), 690 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.34-7.24 (m, 5 H), 4.55 (ABq, J_(AB) =12.1 Hz, Δδ_(AB) =14.4 Hz, 2 H), 4.30 (d, J=2.9 Hz, 1 H), 4.12-4.07 (m, 1 H), 4.01 (ddd, J=9.2, 9.2, 2.7 Hz, 1 H), 3.51 (apparent t, J=4.4 Hz, 1 H), 3.50 (dd, J=9.5, 4.2 Hz, 1 H), 3.39 (dd, J=9.5, 7.1 Hz, 1 H), 3.28 (s, 3 H), 2.86 (d, J=3.2 Hz, 1 H), 1.85 (qdd, J=7.3, 5.2, 2.9 Hz, 1 H), 1.76 (dqd, J=9.3, 6.9, 4.0 Hz, 1 H), 1.71 (ddd, J=14.5, 9.0, 2.8 Hz, 1 H), 1.55 (ddd, J=14.4, 9.2, 2.9 Hz, 1 H), 0.96 (d, J=7.3 Hz, 3 H), 0.88 (s, 9 H), 0.81 (d, J=6.8 Hz, 3 H), 0.03 (s, 3 H), -0.01 (s, 3 H); ¹³ C NMR d 138.2, 128.4, 127.7, 101.2, 76.7, 74.7, 73.3, 73.0, 67.4, 56.7, 41.1, 36.0, 34.7, 25.9, 18.1, 13.7, 9.7, -4.6, -4.9; high resolution mass spectrum (FAB, NBA) m/z 461.2715 [(M+Na)⁺ ; calcd for C₂₄ H₄₂ O₅ SiNa: 461.2699].

EXAMPLE 29 Methyl Pyranoside 36

A solution of 35 (281.2 mg, β/α=2:1, 0.642 mmol) and 2,6-lutidine (224.0 μL, 1.92 mmol) in CH₂ Cl₂ (6.0 mL) was cooled to 0° C. and TBSOTf (295.0 μL, 1.28 mmol) was added over 5 min. After 1 h at 0° C., the mixture was diluted with ethyl acetate (100 mL), washed with aqueous NaHSO₄ (1.0 M, 50 mL), brine (100 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (5% ethyl acetate/hexane) provided 36 (344.6 mg, β/α=2:1, 97% yield) as a colorless oil.

α anomer: [α]²³ _(D) +50.0° ©1.44, CHCl₃); IR (CHCl₃) 2960 (s), 2935 (s), 2885 (s), 2860 (s), 1490 (w), 1460 (m), 1388 (m), 1378 (m), 1360 (m), 1250 (s), 1190 (m), 1145 (m), 1105 (s), 1085 (s), 1050 (s), 1025 (s), 1002 (s), 963 (m), 934 (m), 867 (m), 833 (s), 690 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.32-7.25 (m, 5 H), 4.51 (ABq, J_(AB) =12.1 Hz, Δδ_(AB) =19.7 Hz, 2 H), 4.23 (d, J=4.8 Hz, 1 H), 4.03 (dddd, J=8.0, 5.3, 5.3, 2.5 Hz, 1 H), 3.87 (ddd, J=9.9, 7.8, 1.8 Hz, 1 H), 3.53 (dd, J=7.2, 4.8 Hz, 1 H), 3.39 (dd, J=9.8, 5.6 Hz, 1 H), 3.37 (dd, J=10.0, 5.2 Hz, 1 H), 3.33 (s, 3 H), 1.79 (dqd, J=7.1, 7.1, 4.9 Hz, 1 H), 1.71-1.64 (m, 2 H), 1.53 (ddd, J=14.4, 8.8, 1.9 Hz, 1 H), 0.94 (d, J=7.0 Hz, 3 H), 0.89 (s, 9 H), 0.865 (s, 9 H), 0.862 (d, J=6.9 Hz, 3 H), 0.07 (s, 3 H), 0.04 (s, 3 H), 0.03 (s, 3 H), 0.005 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 138.5, 128.3, 127.6, 127.5, 103.8, 75.5, 73.2, 72.8, 69.8, 69.1, 55.7, 38.9, 38.5, 37.6, 26.0, 25.8, 18.18, 18.16, 15.1, 12.9, -3.9, -4.6, -4.7, -4.8; high resolution mass spectrum (FAB, NBA) m/z 575.3552 [(M+Na)⁺ ; calcd for C₃₀ H₅₆ O₅ Si₂ Na: 575.3564].

β anomer: [α]²³ _(D) +13.3° ©1.38, CHCl₃); IR (CHCl₃) 3003 (m), 2960 (s), 2935 (s), 2880 (s), 2860 (s), 1495 (w), 1470 (m), 1464 (m), 1390 (m), 1360 (m), 1350 (m), 1330 (w), 1253 (s), 1155 (s), 1140 (s), 1120 (s), 1090 (s), 1045 (s), 1022 (s), 1002 (s), 953 (m), 933 (m), 850 (s), 830 (s), 690 (m), 658 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.32-7.22 (m, 5 H), 4.74 (d, J=2.4 Hz, 1 H), 4.50 (ABq, J_(AB) =13.2 Hz, Δδ_(AB) =17.8 Hz, 2 H), 4.23-4.18 (m, 1 H), 3.74 (ddd, J=10.6, 10.6, 1.3 Hz, 1 H), 3.60 (apparent t, J=2.7 Hz, 1 H), 3.48 (s, 3 H), 3.38 (dd, J=9.8, 4.5 Hz, 1 H), 3.35 (dd, J=9.8, 5.7 Hz, 1 H), 1.88 (qdd, J=7.1, 2.7, 2.7 Hz, 1 H), 1.66 (ddd, J=14.0, 10.1, 1.6 Hz, 1 H), 1.63-1.55 (m, 1 H), 1.49 (ddd, J=14.0, 10.8, 1.8 Hz, 1 H), 0.91 (d, J=7.1 Hz, 3 H), 0.89 (s, 9 H), 0.88 (s, 9 H), 0.785 (d, J=6.8 Hz, 3 H), 0.07 (s, 3 H), 0.045 (s, 3 H), 0.040 (s, 3 H), 0.02 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 138.5, 128.2, 127.6, 127.4, 100.6, 76.9, 75.8, 73.2, 71.7, 67.9, 56.7, 41.1, 38.4, 35.0, 26.1, 25.8, 18.2, 18.1, 14.0, 9.7, -3.9, -4.5, -5.0; high resolution mass spectrum (FAB, NBA) m/z 575.3560 [(M+Na)⁺ ; calcd for C₃₀ H₅₆ O₅ Si₂ Na: 575.3564].

EXAMPLE 30 Primary Alcohol 37

A solution of 36 (331.6 mg, 0.600 mmol) in EtOH/EtOAc (1:8, 9 mL) was treated with Pd/C (10% wet, E101 NE/W, 51.2 mg) under H₂ atmosphere for 3 h, then filtered and concentrated. Flash chromatography (10% ethyl acetate/hexane) provided 37 (276.6 mg, β/α=2:1, 99% yield) as a colorless oil.

β anomer: [α]²³ _(D) +16.9° ©2.52, CHCl₃); IR (CHCl₃) 3680 (w), 3590 (w, br), 3450 (w, br), 3000 (m), 2960 (s), 2925 (s), 2880 (m), 2855 (s), 1470 (m), 1462 (m), 1388 (m), 1360 (m), 1253 (s), 1222 (m), 1200 (m), 1150 (m),1130 (m), 1110 (s), 1098 (m), 1065 (s), 1046 (s), 1023 (s), 1002 (m), 980 (m), 952 (m), 894 (m), 865 (m), 850 (m), 830 (s), 663 (m), 657 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 4.73 (d, J=2.5 Hz, 1 H), 4.09-4.05 (m, 1 H), 3.64 (ddd, J=10.5, 10.5, 1.3 Hz, 1 H), 3.60 (apparent t, J=2.5 Hz, 1 H), 3.62-3.59 (m, 1 H), 3.47 (s, 3 H), 3.47-3.42 (m, 1 H), 1.95-1.85 (m, 2 H), 1.82 (ddd, J=14.3, 9.2, 1.5 Hz, 1 H), 1.60 (dqd, J=10.2, 6.8, 2.5 Hz, 1 H), 1.45 (ddd, J=14.3, 10.7, 2.6 Hz, 1 H), 0.895 (d, J=7.5 Hz, 3 H), 0.887 (apparent s, 18 H), 0.785 (d, J=6.8 Hz, 3 H), 0.09 (s, 3 H), 0.08 (s, 3 H), 0.04 (s, 3 H), 0.02 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 100.8, 76.8, 72.2, 69.5, 67.6, 56.8, 41.0, 38.2, 34.9, 25.9, 25.8, 18.1, 14.0, 9.7, -4.2, -4.6, -4.7, -5.0; high resolution mass spectrum (FAB, NBA) m/z 485.3080 [(M+Na)⁺ ; calcd for C₂₃ H₅₀ O₅ SiNa: 485.3094].

α anomer: [α]²³ _(D) +54.9° ©1.20, CHCl₃); IR (CHCl₃) 3670 (w), 3590 (w) 3440 (w, br), 3000 (m), 2960 (s), 2925 (s), 2880 (m), 2855 (s), 1463 (m), 1390 (m), 1360 (m), 1255 (s), 1225 (m), 1192 (m), 1168 (m), 1143 (m), 1102 (s), 1083 (s),1045 (s), 1030 (m), 1002 (m), 963 (m), 932 (m), 862 (m), 833 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 4.25 (d, J=4.2 Hz, 1 H), 3.89 (dddd, J=6.5, 4.6, 4.6, 4.6 Hz, 1 H), 3.80 (ddd, J=9.1, 9.1, 2.3 Hz, 1 H), 3.61 (br dd, J=10.9, 3.4 Hz, 1 H), 3.51 (dd, J=6.5, 4.6 Hz, 1 H), 3.52-3.48 (m, 1 H), 3.33 (s, 3 H), 2.15 (s, br, 1 H), 1.81 (dqd, J=6.9, 6.9, 4.2 Hz, 1 H), 1.72-1.60 (m, 3 H), 0.94 (d, J=7.1 Hz, 3 H), 0.882 (s, 9 H), 0.879 (s, 9 H), 0.845 (d, J=6.8 Hz, 3 H), 0.09 (s, 3 H), 0.08 (s, 3 H), 0.02 (s, 3 H), 0.00 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 104.0, 72.7, 71.3, 70.0, 67.6, 55.7, 38.7, 38.5, 37.3, 25.8, 18.13, 18.08, 15.2, 13.1, -4.4, -4.6, -4.7; high resolution mass spectrum (FAB, NBA) m/z 485.3081 [(M+Na)⁺ ; calcd for C₂₃ H₅₀ O₅ Si₂ Na: 485.3094].

EXAMPLE 31 Alcohol 38

A solution of 37 (276.6 mg, 0.598 mmol) in Et₂ O (40 mL) was treated with EtSH (8.90 mL, 120 mmol) and MgBr₂.Et₂ O (1.54 g, 5.96 mmol) at room temperature. After 60 h, the mixture was diluted with ethyl acetate (50 mL), washed with brine (2×100 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (3% acetone/hexane) provided 38 α (34.4 mg, 12% yield) and 38 β (211.3 mg, 71% yield).

β anomer: colorless oil; [α]²³ _(D) +16.6° ©1.18, CHCl₃); IR (CHCl₃) 3595 (m), 3400 (m, br), 3000 (m), 2960 (s), 2930 (s), 2855 (s), 1655 (w), 1612 (s), 1588 (m), 1510 (s), 1462 (s), 1375 (m), 1360 (m), 1300 (m), 1250 (s, br), 1170 (m), 1080 (s, br), 1030 (s), 1002 (m), 967 (m), 835 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 5.08 (d, J=2.3 Hz, 1 H), 4.04-4.00 (m, 1H), 3.62 (ddd, J=10.4, 10.4, 1.0 Hz, 1 H), 3.60 (ddd, J=11.1, 11.1, 4.2 Hz, 1 H), 3.56 (apparent t, J=2.7 Hz, 1 H), 3.43 (ddd, J=11.7, 7.9, 4.1 Hz, 1 H), 2.70 (dq, J=12.7, 7.4 Hz, 1 H), 2.67 (dq, J=12.8, 7.5 Hz, 1 H), 1.95 (dd, J=7.9, 4.8 Hz, 1 H), 1.86 (qdd, J=7.1, 2.7, 2.7 Hz, 1 H), 1.79 (ddd, J=14.4, 9.0, 1.4 Hz, 1 H), 1.66-1.59 (m, 1 H), 1.57 (s, 3 H), 1.45 (ddd, J=14.4, 10.5, 2.7 Hz, 1 H), 1.27 (apparent t, J=7.4 Hz, 1 H), 0.99 (d, J=7.1 Hz, 3 H), 0.90 (s, 9 H), 0.89 (s, 9 H), 0.79 (d, J=6.8 Hz, 3 H), 0.083 (s, 3 H), 0.075 (s, 3 H), 0.04 (s, 3 H), 0.03 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 81.0, 76.2, 75.0, 69.8, 67.6, 41.9, 38.3, 34.5, 25.9, 25.8, 25.2, 18.1, 15.2, 14.4, 11.5, -4.2, -4.56, -4.63, -4.9; high resolution mass spectrum (FAB, NBA) m/z 515.3037 [(M+Na); calcd for C₂₄ H₅₂ O₄ SSi₂ Na: 515.3023].

α anomer: colorless oil; [α]²³ _(D) +94.5° ©0.33, CHCl₃); IR (CHCl₃) 3680 (w), 3580 (w), 3440 (w, br), 3010 (m), 2960 (s), 2930 (s), 2880 (m), 2860 (s), 1513 (w), 1470 (m), 1462 (m), 1390 (m), 1380 (m), 1360 (m), 1257 (s), 1225 (m), 1200 (m), 1114 (m), 1070 (s), 1047 (s), 1022 (m), 1002 (m), 957 (m), 860 (m), 833 (s), 705 (s), 660 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 4.76 (d, J=3.1 Hz, 1 H), 4.04 (ddd, J=9.8, 9.8, 1.8 Hz, 1 H), 3.84 (dddd, J=5.0, 5.0, 5.0, 5.0 Hz, 1 H), 3.57 (dd, J=11.0, 4.2 Hz, 1 H), 3.53 (apparent t, J=4.0 Hz, 1 H), 3.47 (dd, J=11.0, 4.7 Hz, 1 H), 2.57 (dq, J=12.8, 7.5 Hz, 1 H), 2.54 (dq, J=12.8, 7.5 Hz, 1 H), 1.97-1.91 (m, 1 H), 1.75 (ddd, J=14.7, 6.1 Hz, 2.0, 1 H), 1.72-1.65 (m, 1 H), 1.60 (ddd, J=14.9, 10.0, 5.1 Hz, 1 H), 1. 60-1.50 (br, 1 H), 1.23 (apparent t, J=7.4 Hz, 3 H), 1.06 (d, J=7.1 Hz, 3 H), 0.92 (s, 9 H), 0.89 (s, 9 H), 0.85 (d, J=6.9 Hz, 3 H), 0.12 (s, 3 H), 0.08 (s, 3 H), 0.05 (s, 3 H), 0.02 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 85.3, 73.8, 71.5, 69.2, 67.5, 40.6, 38.2, 36.4, 26.4, 26.1, 25.9, 18.2, 18.1, 17.5, 14.7, 13.9, -4.2, -4.4, -4.8; high resolution mass spectrum (FAB, NBA) m/z 515.3045 [(M+Na)⁺ ; calcd for C₂₄ H₅₂ O₄ SSi₂ Na: 515.3023].

EXAMPLE 32 Fragment (+)-C

A solution of DMSO (100 μL, 1.42 mmol) in CH₂ Cl₂ (2.0 mL) was cooled to -78° C. and oxalyl chloride (55.0 μl, 0.630 mmol) was introduced dropwise. After 15 min. a cooled (-78° C.) solution of 38 α (104.8 mg, 0.213 mmol) in CH₂ Cl₂ (1.0 mL) was introduced via cannula (2×500 μL rinse). The resultant milky solution was stirred for 15 min at -78° C. and I-Pr₂ NEt (370 μl, 2.12 mmol) was added dropwise. The reaction mixture was stirred for 0.5 h, slowly warmed to room temperature (15 min), and quenched with aqueous NaHSO₄ (1.0 M, 4.0 mL). The organic phase was diluted with ether (30 mL), washed with brine (3×30 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (2% ethyl acetate/hexane) furnished (+)-C (88.8 mg, 86% yield) as a colorless oil: [α]²³ _(D) +11.2° ©1.42, CHCl₃); IR (CHCl₃) 2960 (s), 2935 (s), 2880 (s), 2860 (s), 1735 (s), 1470 (m), 1460 (m), 1380 (m), 1360 (m), 1320 (m), 1295 (w), 1265 (s), 1153 (m), 1120 (m), 1080 (m), 1060 (s), 1043 (s), 1025 (s), 1003 (s), 970 (m), 950 (m), 935 (m), 903 (m), 865 (m), 835 (s), 800 (m), 690 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 9.56 (d, J=0.9 Hz, 1 H), 5.07 (d, J=2.3 Hz, 1 H), 4.35 (ddd, J=7.9, 2.2, 0.6 Hz, 1 H), 3.70 (ddd, J=10.3, 10.3, 1.5 Hz, 1 H), 3.57 (apparent t, J=2.7 Hz, 1 H), 2.71-2.60 (m, 2 H), 1.86 (apparent qt, J=7.1, 2.7 Hz, 1 H), 1.78 (ddd, J=14.1, 10.4, 7.8 Hz, 1 H), 1.72-1.66 (m, 1 H), 1.67 (ddd, J=10.3, 3.9, 1.8 Hz, 1 H), 1.25 (apparent t, J=7.4 Hz, 3 H), 1.00 (d, J=7.2 Hz, 3 H), 0.90 (s, 9 H), 0.89 (s, 9 H), 0.78 (d, J=6.8 Hz, 3 H), 0.10 (s, 3 H), 0.04 (s, 6 H), 0.03 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 202.6, 81.2, 76.1, 74.9, 73.7, 41.9, 35.8, 34.4, 25.82, 25.79, 25.2, 18.2, 18.1, 15.3, 14.3, 11.5, -4.2, -4.5, -4.9, -5.2; high resolution mass spectrum (CI, NH₃) m/z 491.3058 [(M+H)⁺ ; calcd for C₂₄ H₅₁ O₄ SSi₂ : 491.3046].

EXAMPLE 33

Fragment (-)-B

From vinyl bromide (-)-22: A solution of (-)-22 (3.78 g, 8.04 mmol) in HMPA/DMF (2:1, 6 mL) was added to a mixture of KI (4.15 g, 250 mmol), NiBr₂ (34.9 mg, 0.160 mmol), and Zn powder (23.2 mg, 0.355 mmol). The mixture was stirred at room temperature for 15 min then heated to 90 ° C. The green color mixture turned black-brown after 5 min and dark green after 1 h. After additional 1 h at 90° C., the mixture was cooled to room temperature, diluted with ethyl acetate (200 mL), washed with brine (4×200 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (2% ethyl acetate/hexane) provided B (3.59 g, containing 13% unreacted vinyl bromide) as a colorless oil.

From aldehyde (+)-18: A suspension of EtPh₃ P⁺ I⁻ (15.1 g, 36.1 mmol) in THF (200 mL) was treated with n-BuLi (1.6 M in hexane, 23.0 mL, 36.8 mmol) at room temperature over 10 min. After an additional 10 min, the resultant red solution was added via cannula to a cooled (-78° C.) solution of I₂ (8.02 g, 31.6 mmol) in THF (300 mL) over 15 min. The yellow slurry formed was stirred at -78° C. for 5 min and at -23° C. for 10 min. NaHMDS (1.0 M in THF, 31.0 mL, 31.0 mmol) was added over 8 min and the mixture stirred 15 min further. A solution of aldehyde (+)18 (6.96 g, 18.3 mmol) in THF (50 mL) was introduced via cannula (10 mL rinse), and the reaction mixture was stirred at -23° C. for 10 min, warmed to room temperature, stirred for 3 h, and then quenched with MeOH (10 mL). Following concentration and filtration through a silica column (50% ethyl acetate/hexane), the filtrate was washed with saturated aqueous Na₂ S₂ O₃, brine (300 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (5% ethyl acetate/hexane) furnished B (6:1 Z/E, 3.94 g, 41% yield) as a colorless oil.

An analytical sample of (-)-B was obtained by reversed-phase HPLC (gradient elution, 90% CH₃ CN/H₂ O →100% CH₃ CN) : [α]²³ _(D) 23°©0.30, CHCl₃); IR (CHCl₃) 3000 (m) , 2960 (s), 2930 (s), 2880 (m), 2855 (s), 1610 (m), 1588 (w), 1510 (s), 1463 (m), 1453 (m), 1428 (m), 1405 (w), 1390 (m), 1377 (m), 1360 (m), 1303 (m), 1250 (s), 1180 (m), 1172 (m), 1080 (s, br), 1033 (s), 1002 (m), 948 (m), 935 (m), 922 (m), 833 (s), 803 (m), 760 (m, br), 720 (m), 658 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.25 (d, J=8.6 Hz, 2 H), 6.87 (d, J=8.7 Hz, 2 H), 5.28 (apparent dd, J=8.9, 1.4 Hz, 1 H), 4.41 (ABq, J_(AB) =7.0 Hz, Δδ_(AB) =10.2 Hz, 2 H), 3.80 (s, 3 H), 3.60 (apparent t, J=5.3 Hz, 1 H), 3.51 (dd, J=9.1, 5.1 Hz, 1 H), 3.23 (dd, J=9.0, 8.0 Hz, 1 H), 2.54-2.47 (m, 1 H), 2.44 (d, J=1.4 Hz, 3 H), 2.00-1.92 (m, 1 H), 1.00 (d, J=6.9 Hz, 3 H), 0.95 (d, J=6.7 Hz, 3 H), 0.89 (s, 9 H), 0.02 (s, 3 H), 0.01 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.1, 139.6, 131.0, 129.1, 113.7, 98.9, 76.5, 72.6, 72.5, 55.3, 44.5, 38.7, 33.5, 26.1, 18.4, 20 14.7, 14.5, -3.95, -3.99; high resolution mass spectrum (FAB, NBA) m/z 541.1626 [(M+Na)⁺ ; calcd for C₂₃ H₃₉ O₃ ISiNa: 541.1611].

EXAMPLE 34

Olefin (-)-39

ZnCl₂ (1.32 g, 9.69 mmol) was dried at 160° C. under vacuum overnight and then treated with a solution of (-)-A (5.25 g, 9.59 mmol) in dry Et₂ O (50 mL) via a cannula (2×25 mL rinse). The mixture was stirred at room temperature until most of the ZnCl₂ dissolved and cooled to -78° C. t-BuLi (1.7 M in pentane, 17.0 mL) was added over 30 min, and the resultant solution was stirred 15 min further, warmed to room temperature, and stirred for 1 h. The solution was added by cannula to a mixture of B (3.21 g, 6.19 mmol; 6:1 Z/E) and Pd(PPh₃)₄ (364.0 mg, 0.315 mmol). The mixture was covered with aluminum foil, stirred overnight, and then diluted with ethyl acetate (100 mL), washed with brine (2×100 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (5% ethyl acetate/hexane) gave (-)-39 (3.32 g, 66% yield) as a white semisolid: [α]²³ _(D) -28.6°©1.53, CHCl₃); IR (CHCl₃) 3010 (m), 2970 (s), 2940 (s), 2865 (s), 1620 (m), 1590 (w), 1520 (s), 1465 (s), 1445 (m), 1390 (m), 1380 (m), 1360 (m), 1305 (m), 1250 (s), 1175 (m), 1115 (s), 1080 (s), 1040 (s), 970 (m), 940 (w), 860 (m), 835 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.36 (d, J=8.7 Hz, 2 H), 7.22 (d, J=8.6 Hz, 2 H), 6.86 (d, J=9.0 Hz, 2 H), 6.84 (d, J=8.9 Hz, 2 H), 5.37 (s, 1 H), 5.00 (d, J=10. 2 Hz, 1 H), 4.36 (ABq, J_(AB) =11.6 Hz, Δδ_(AB) =17.4 Hz, 2 H), 4.08 (dd, J=11.2, 4.7 Hz, 1 H), 3.78 (s, 3 H), 3.77 (s, 3 H), 3.61 (dd, J=7.1, 1.8 Hz, 1 H), 3.51 (dd, J=9.9, 1.7 Hz, 1 H), 3.47 (apparent t, J=11.0 Hz, 1 H), 3.46 (dd, J=9.1, 5.0 Hz, 1 H), 3.38 (dd, J=6.0, 4.8 Hz, 1 H), 3.19 (apparent t, J=8.8 Hz, 1 H), 2.51 (ddq, J=10.1, 6.5, 6.5 Hz, 1 H), 2.32 (apparent t, J=12.2 Hz, 1 H), 2.08-2.02 (m, 1 H), 1.99-1.93 (m, 2 H), 1.88 (dqd, J=7.1, 7.1, 1.8 Hz, 1 H), 1. 67 (br d, J=11.1 Hz, 1 H), 1.55 (d, J=0.5 Hz, 3 H), 1.01 (d, J=7.1 Hz, 3 H), 0.94 (d, J=6.9 Hz, 3 H), 0.90 (s, 9 H), 0.89 (d, J=6.7 Hz, 3 H), 0.87 (s, 9 H), 0.74 (d, J=6.3 Hz, 3 H), 0.73 (d, J=6.4 Hz, 3 H), 0.03 (s, 3 H), 0.013 (s, 3 H), 0.008 (s, 3 H), 0.003 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.8, 159.0, 132.0, 131.5, 131.2, 131.1, 129.0, 127.3, 113.7, 113.5, 101.1, 83.4, 78.49, 78.46, 73.3, 72.6, 72.5, 55.3, 38.8, 38.2, 37.5, 35.6, 33.7, 30.8, 26.27, 26.25, 23.1, 18.42, 18.40, 17.0, 14.6, 12.6, 12.1, 10.9, -3.5, -3.7, -3.8, -3.9; high resolution mass spectrum (FAB, NBA) m/z 835.5315 [(M+Na)⁺ ; calcd for C₄₇ H₈₀ O₇ Si₂ Na: 835.5341].

Anal. Calcd for C₄₇ H₈₀ O₇ Si₂ : C, 69.41; H, 9.91. Found: C, 69.52; H, 10.10.

EXAMPLE 35

Alcohol (-)-40

A solution of olefin (-)-39 (2.65 g, 3.26 mmol) in CH₂ Cl₂ (32 mL) was cooled to 0° C. and treated with H₂ O (1.50 mL) and DDQ (774 mg, 3.41 mmol). After 4 h, the mixture was diluted with CH₂ Cl₂ (20 mL), dried over MgSO₄, and filtered through a silica column (50% ethyl acetate/hexane). Following concentration, the residue was dissolved in EtOH (50 mL) and treated with NaBH₄ (500 mg, excess) at room temperature to reduce the contaminated p-methoxybenzyl aldehyde. After 0.5 h, the mixture was quenched with saturated aqueous NH₄ Cl (50 mL) at 0° C. then concentrated. The residue was partitioned between CH₂ Cl₂ (200 mL) and water (100 mL). The organic phase was washed with water (100 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (10% ethyl acetate/hexane) provided (-)-40 (2.06 g, 91% yield) as a white solid. mp 99-100° C.; [α]²³ _(D) -25.4°©1.35, CHCl₃); IR (CHCl₃) 3520 (w), 3010 (m), 2960 (s), 2940 (s), 2880 (m), 2860 (m), 1620 (m), 1593 (w), 1520 (m), 1565 (m), 1390 (m), 1360 (m), 1255 (s), 1175 (m), 1165 (m), 1117 (m), 1075 (s), 1037 (s), 1025 (s), 1005 (m), 982 (m), 965 (m), 930 (w), 835 (s), 800 (m), 705 (w), 675 (w), 660 (w) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.36 (d, J=8.7 Hz, 2 H), 6.86 (d, J=8.8 Hz, 2 H), 5.37 (s, 1 H), 5.01 (d, J=10.1 Hz, 1 H), 4.09 (dd, J=11.2, 4.7 Hz, 1 H), 3.79 (s, 3 H), 3.65 (dd, J=10.4, 4.7 Hz, 1 H), 3.63 (dd, J=7.0, 1.8 Hz, 1 H), 3.54-3.50 (m, 1 H), 3.51 (dd, J=10.0, 2.0 Hz, 1 H), 3.47 (apparent t, J=11.2 Hz, 1 H), 3.41 (dd, J=6.6, 4.0 Hz, 1 H), 2.59 (ddq, J=13.2, 6.7, 6.7 Hz, 1 H), 2.33 (apparent t, J=12.2 Hz, 1 H), 2.24 (apparent t, J=5.5 Hz, 1 H), 2.09-1.95 (m, 2 H), 1.89 (dqd, J=7.0, 7.0, 1.7 Hz, 1 H), 1.84-1.77 (m, 1 H), 1.72 (br d J=11.0 Hz, 1 H), 1.58 (d, J=0.8 Hz, 3 H), 1.01 (d, J=7.1 Hz, 3 H), 0.98 (d, J=7.1 Hz, 3 H), 0.94 (d, J=6.7 Hz, 3 H), 0.910 (s, 9 H), 0.905 (s, 9 H), 0.75 (d, J=7.1 Hz, 3 H), 0.74 (d, J=7.1 Hz, 3 H), 0.09 (s, 3 H), 0.07 (s, 3 H), 0.05 (s, 3 H), 0.01 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.8, 133.0, 131.5, 130.5, 127.3, 113.4, 101.0, 83.3, 81.6, 78.4, 73.3, 65.4, 55.3, 38.5, 38.2, 37.6, 37.0, 33.7, 30.8, 26.17, 26.16, 23.2, 18.4, 18.3, 17.4, 15.7, 12.6, 12.1, 10.9, -3.57, -3.61, -3.66, -3.9; high resolution mass spectrum (CI, NH₃) m/z 693.4918 [(M+H)⁺ ; calcd for C₃₉ H₇₃ O₆ Si₂ : 693.4945].

Anal. Calcd for C₃₉ H₇₂ 0₆ Si₂ : C, 67.58; H, 10.47. Found: C, 67.30; H, 10.54.

EXAMPLE 36

Phosphonium Salt (-)-49

A solution of alcohol (-)-40 (402.8 mg, 0.577 mmol) in PhH/Et₂ O (1:2, 45 mL) was treated with PPh₃ (532 mg, 2.03 mmol) and imidazole (158 mg, 2.32 mmol). After the imidazole dissolved, I₂ (437 mg, 1.72 mmol) was added under vigorous stirring. The mixture was stirred 2 h and then treated with NEt₃ (2 mL). The resultant yellow suspension was diluted with CH₂ Cl₂ (50 mL) and washed with saturated aqueous Na₂ S₂ O₃ (100 mL), saturated aqueous NaHCO₃ (100 mL), and brine (2×100 mL). The organic phase was dried over MgSO₄, filtered and concentrated. Filtration through a short silica column (NEt₃ /ethyl acetate/hexane, 2:10:90) removed triphenylphosphine oxide, affording the impure iodide 42. Preparative TLC (500 mm silica gel plate, 4% acetone/hexane) furnished an analytical sample as an unstable white solid: ¹ H NMR (500 MHZ, CDCl₃) d 7.35 (d, J=8.8 Hz, 2 H), 6.85 (d, J=8.7 Hz, 2 H), 5.37 (s, 1 H), 5.02 (d, J=10.2 Hz, 1 H), 4.08 (dd, J=11.2, 4.7 Hz, 1 H), 3.78 (s, 3 H), 3.62 (dd, J=7.0, 1.8 Hz, 1 H), 3.51 (dd, J=9.9, 1.7 Hz, 1 H), 3.47 (apparent t, J=11.1 Hz, 1 H), 3.37 (dd, J=6.3, 4.3 Hz, 1 H), 3.32 (dd, J=9.6, 4.5 Hz, 1 ), 2.99 (dd, J=9.5, 8.6 Hz, 1 H), 2.50 (ddq, J=10.2, 6.5, 6.5 Hz, 1 H), 2.31 (apparent t, J=12.2 Hz, 1 H), 2.08-1.95 (m, 2 H), 1.88 (dqd, J=7.1, 7.1, 1.7 Hz, 1 H), 1.85-1.78 (m, 1 H), 1.74 (br d, J=11.7 Hz, 1 H), 1.57 (apparent s, 3 H), 1.01 (apparent d, J=7.0 Hz, 6 H), 0.91-0.89 (m, 3 H), 0.90 (s, 9 H), 0.89 (s, 9 H), 0.74 (d, J=6.8 Hz, 3 H), 0.73 (d, J=6.7 Hz, 3 H), 0.06 (s, 3 H), 0.05 (s, 3 H), 0.01 (s, 3 H), -0.02 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃ /1% pyridine-d₅, 20 mg sample) d 159.8, 132.9, 131.5, 130.4, 127.3, 113.5, 101.1, 83.3, 79.6, 78.5, 73.3, 55.3, 41.4, 38.3, 37.6, 36.0, 33.7, 30.8, 26.20, 26.17, 23.2, 18.4, 17.7, 17.3, 13.5, 12.6, 12.2, 10.9, -3.5, -3.6, -4.0; high resolution mass spectrum (FAB, 10 NBA) m/z 803.3935 [(M+H)⁺ ; calcd for C₃₉ H₇₂ O₅ ISi₂ : 803.3963].

The very sensitive impure iodide (obtained by filtration through silica) was quickly mixed with I--Pr₂ NEt (300 μL, 1.72 mmol) and PPh₃ (2.47 g, 9.42 mmol). The mixture was heated at 80° C. for 24 h, then cooled to room temperature and extracted with hexane (2×30 mL). The residue was purified by flash chromatography (2% MeOH/CHCl₃) furnishing (-)-49 (224.9 mg, 37% yield from (-)-39) as a pale yellow foam. The hexane extract was concentrated and purified by flash chromatography (2% ethyl acetate/hexane) affording a mixture of cyclization products (200 mg). Further purification by normal phase HPLC (1.5% ethyl acetate/hexane) provided (-)-50 as the major cyclization product.

Wittig reagent (-)-49: [α]²³ _(D) -25.3°©1.48, CHCl₃); IR (CHCl₃) 2960 (s), 2930 (s), 2860 (m), 1615 (m), 1590 (w), 1515 (m), 1485 (w), 1460 (m), 1440 (m), 1385 (m), 1360 (m), 1300 (m), 1250 (s), 1215 (m, br), 1180 (m), 1110 (s), 1080 (m), 1025 (m), 1005 (m), 965 (m), 945 (w), 860 (m), 830 (s), 732 (m), 725 (m), 710 (m), 680 (m), 653 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃ ; concentration dependent) d 7.82-7.76 (m, 15 H), 7.35 (d, J=8.8 Hz, 2 H), 6.84 (d, J=8.8 Hz, 2 H), 5.35 (s, 1 H), 5.30 (d, J=10.5 Hz, 1 H), 4.07 (dd, J=11.2, 4.7 Hz, 1 H), 3.77 (s, 3 H), 3.73-3.67 (m, 2 H), 3.56 (dd, J=7.0, 1.8 Hz, 1 H), 3.48 (dd, J=9.8, 1.7 Hz, 1 H), 3.46 (apparent t, J=11.1 Hz, 1 H), 3.31 (ddd, J=15.6, 11.2, 11.2 Hz, 1 H), 2.49 (ddq, J=10.5, 6.4, 6.4 Hz, 1 H), 2.25 (apparent t, J=12.1 Hz, 1 H), 2.10-1.92 (m, 3 H), 1.85 (dqd, J=7.1, 7.1, 1.8 Hz, 1 H), 1.57-1.52 (m, 1 H), 1.56 (s, 3 H), 0.98 (d, J=7.1 Hz, 3 H), 0.89 (d, J=6.6 Hz, 3 H), 0.852 (s, 9 H), 0.849 (s, 9 H), 0.72-0.71 (m, 3 H), 0.71 (d, J=6.6 Hz, 3 H), 0.69 (d, J=6.9 Hz, 3 H), 0.10 (s, 3 H), -0.02 (s, 3 H), -0.03 (s, 3 H), -0.07 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.8, 135.2 (J_(CP) =2.6 Hz), 133.5 (J_(CP) =10.0 Hz), 132.9, 131.4, 130.6 (J_(CP) =12.6 Hz), 130.3, 127.3, 118.4 (J_(CP) =85.5 Hz), 113.4, 101.0, 83.2, 80.1 (J_(CP) =14.0 Hz), 78.3, 73.2, 55.3, 38.1, 37.4, 36.0, 33.7 (J_(CP) =4.4 Hz), 33.6, 30.7, 26.1, 25.5 (J_(CP) =49.7 Hz), 22.9, 18.33, 18.29, 17.2, 17.1, 12.5, 12.1, 10.9, -3.2, -3.6, -3.7, -4.0; high resolution mass spectrum (FAB, NBA) m/z 937.5708 [(M-I)⁺ ; calcd for C₅₇ H₈₆ O₅ PSi₂ : 937.5751].

Olefin (-)50: white solid; mp 80-82° C.; [α]²³ _(D) -18°©0.48, CHCl₃); IR (CHCl₃) 2955 (s), 2920 (s), 2880 (m), 2850 (s), 1640 (w), 1613 (m), 1588 (w), 1517 (m), 1460 (m), 1387 (m), 1360 (m),1300 (m), 1250 (s), 1178 (m), 1170 (m), 1160 (m), 1115 (m), 1080 (m), 1023 (s), 1000 (m), 980 (m), 960 (m), 930 (w), 887 (m), 855 (m), 830 (m), 715 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, C₆ D₆) d 7.62 (d, J=8.7 Hz, 2 H), 6.83 (d, J=8.7 Hz, 2 H), 5.46 (s, 1 H), 5.00 (s, 1 H), 4.95 (s, 1 H), 3.93 (dd, J=11.1, 4.7 Hz, 1 H), 3.89 (dd, J=7.2, 1.5 Hz, 1 H), 3.55 (dd, J=9.9, 1.9 Hz, 1 H), 3.51 (apparent t, J=5.9 Hz, 1 H), 3.27 (s, 3 H), 3.22 (apparent t, J=11.0 Hz, 1 H), 2.32 (dd, J=13.6, 3.5 Hz, 1 H), 2.27-2.20 (m, 1 H), 2.16 (dd, J=13.7, 9.5 Hz, 1 H), 2.07-1.92 (m, 4 H), 1.87-1.80 (m, 1 H), 1.50-1.42 (m, 1 H), 1.18 (d, J=7.1 Hz, 3 H), 1.10 (d, J=6.6 Hz, 3 H), 1.06 (d, J=6.6 Hz, 3 H), 1.04 (s, 9 H), 1.02 (d, J=7.0 Hz, 3 H), 1.00 (s, 9 H), 0.41 (d, J=6.7 Hz, 3 H), 0.13 (s, 3 H), 0.09 (s, 3 H), 0.08 (s, 3 H), 0.06 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.8 (q), 150.7 (q), 131.5 (q), 127.3, 113.4, 108.3 (CH₂), 101.0, 83.2, 81.9, 78.1, 73.3 (CH₂), 55.2, 49.9, 44.9, 41.4 (CH₂), 39.0 (CH₂), 38.3, 36.6, 33.4, 30.8, 26.3, 25.9, 18.5 (q), 18.2 (q), 17.8, 15.5, 12.9, 12.1, 11.0, -3.4, -3.7, -4.6, -4.7; high resolution mass spectrum (FAB, NBA) m/z 697.4642 [(M+Na)⁺ ; calcd for C₃₉ H₇₀ O₅ SI₂ Na: 697.4659].

EXAMPLE 37

Model Olefin (+)-43

NaHMDS (0.6 M in PhMe, 9.46 mL, 5.68 mmol) was added over 10 min to a suspension of (CH₃)₂ CHP⁺ Ph₃ I⁻ (2.52 g, 5.83 mmol) in PhMe (20 mL) at room temperature. After 15 min, the mixture was cooled to -78° C., and aldehyde (+)18 (1.46 g, 3.84 mmol) in PhMe (15 mL) was introduced via a cannula (15mL rinse). After 20 min at -78° C. and 30 min at room temperature, the reaction was quenched with MeOH (1.0 mL). The solution was separated, and the oil residue was extracted with hexane (3×30 mL). The combined organic solutions were then concentrated and, and flash chromatography (2% ethyl acetate/hexane) provided (+)-43 (1.44 g, 92% yield) as a colorless oil: [α]²³ _(D+) 8.07°©2.57, CHCl₃); IR (CHCl₃) 2960 (s), 2925 (s), 2880 (s), 2855 (s), 1610 (m), 1585 (m), 1510 (s), 1460 (s), 1375 (m), 1360 (m), 1300 (m), 1245 (s), 1172 (m), 1085 (s, br), 1035 (s), 1003 (m), 970 (m), 950 (m), 935 (m), 862 (s), 835 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.23 (d, J=9.0 Hz, 2 H), 6.85 (d, J=8.6 Hz, 2 H), 4.92 (d-quintet, J=9.7, 1.4 Hz, 1 H), 4.37 (apparent s, 2 H), 3.78 (s, 3 H), 3.49 (dd, J=9.2, 4.9 Hz, 1 H), 3.39 (dd, J=6.3, 4.5 Hz, 1 H), 3.19 (dd, J=9.0, 8.4 Hz, 1 H), 2.49 (ddq, J=9.6, 6.7, 6.7 Hz, 1 H), 2.00-1.92 (m, 1 H), 1.63 (d, J=1.2 Hz, 3 H), 1.55 (d, J=1.3 Hz, 3 H), 0.945 (d, J=7.0 Hz, 3 H), 0.874 (d, J=6.7 Hz, 3 H), 0.873 (s, 9 H), 0.01 (apparent s, 6 H); 1³ C NMR (125 MHZ, CDCl₃) 159.0, 131.1, 129.7, 129.4, 129.1, 113.7, 78.6, 72.6, 55.3, 38.5, 36.0, 26.2, 25.8, 18.4, 17.9, 17.0, 14.8, -3.88, -3.95; high resolution mass spectrum (CI, NH₃) m/z 407.2984 [(M+H)⁺ ; calcd for C₂₄ H₄₃ O₃ Si: 407.2981].

EXAMPLE 38

Alcohol (+)-44

A mixture of olefin (+)-43 (387.6 mg, 0.954 mmol) in CH₂ Cl₂ (10 mL) was treated with H₂ O (500 μL) and DDQ (320 mg, 1.41 mmol). After 30 min at room temperature, the mixture was filtered through a short silica plug (50% ethyl acetate/hexane) and concentrated. Flash chromatography (3% ethyl acetate/hexane) provided (+)-43 (273.1 mg, 99% yield) as a colorless oil: [α]23_(D) +17.50°©2.80, CHCl₃); IR (CHCl₃) 3620 (w), 3500 (m, br), 2955 (s), 2925 (s), 2880 (s), 2860 (s), 1460 (s), 1405 (m), 1375 (m), 1360 (m), 1337 (m), 1252 (s), 1070 (s), 1050 (s), 1015 (s), 1002 (s), 978 (m), 933 (m), 832 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 4.92 (apparent d quintet, J=9.7, 1.4 Hz, 1 H), 3.66 (ddd, J=11.0, 4.4, 4.4 Hz, 1 H), 3.52 (ddd, J=11.0, 5.5, 5.5 Hz, 1 H), 3.42 (dd, J=6.8, 4.0 Hz, 1 H), 2.57 (ddq, J=9.6, 6.8, 6.8 Hz, 1 H), 2.45 (apparent t, J=5.2 Hz, 1 H), 1.85-1.78 (m, 1 H), 1.65 (d, J=1.3 Hz, 3 H), 1.59 (d, J=1.3 Hz, 3 H), 0.98 (d, J=7.1 Hz, 3 H), 0.92 (d, J=6.8 Hz, 3 H), 0.90 (s, 9 H), 0.08 (s, 3 H), 0.05 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 130.7, 128.5, 81.7, 65.5, 38.1, 37.4, 26.2, 25.8, 18.3, 17.9, 17.4, 15.9, -3.7, -3.9; high resolution mass spectrum (CI, NH₃) m/z 287.2418 [(M+H)⁺ ; calcd for C₁₆ H₃₅ O₂ Si: 287.2406].

EXAMPLE 39

Wittig reagent (+)-46

Iodine (1.08 g, 4.24 mmol) was added to a solution of alcohol (+)-44 (810 mg, 2.83 mmol), PPh₃ (1.11 g, 4.24 mmol) and imidazole (289 mg, 4.24 mmol) in benzene/ether (1:2, 21 mL) under vigorous stirring at room temperature. After 40 min, the mixture was diluted with ether (100 mL), washed with saturated Na₂ S₂ O₃ (50 mL), brine (100 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (hexane) provided a mixture of 45/47/48 (1.06 g, 97% yield, 18:1:1) as a colorless oil; This material was then treated with I--Pr₂ NEt (928 μL, 5.33 mmol) and PPh₃ (7.01 g, 26.7 mmol) then heated at 80° C. for 13 h. The mixture was extracted with hexane (3×100 mL). The residue was purified by flash chromatography (2% MeOH/CHCl₃) providing Wittig reagent (+)-48 (207.1 mg, 38% yield from (+)-46) as a pale yellow foam. The hexane extract was concentrated and purified by flash chromatography (hexane) affording a mixture of two cyclization products (380 mg) and further purification by preparative TLC (hexane) afforded (-)-49 and (-)-50.

Wittig reagent (+)-46: [α]²³ _(D) +4.80°©1.23, CHCl₃); IR (CHCl₃) 2940 (s), 2860 (m), 1588 (w), 1482 (w), 1468 (m), 1460 (m) , 1440 (s) , 1380 (m) , 1360 (w) , 1310 (w) , 1253 (m) , 1230 (m), 1210 (m), 1110 (s), 1080 (m), 1050 (m), 1018 (m), 1000 (m), 995 (m), 860 (m), 832 (s), 800 (m), 708 (m), 680 (m), 652 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃ ; concentration dependent) d 7.81-7.67 (m, 15 H), 4.92 (d, J=9.7 Hz, 1 H), 3.50 (apparent t, J=5.3 Hz, 1 H), 3.38 (ddd, J=14.9, 14.9, 1.5 Hz, 1 H), 3.25 (ddd, J=15.6, 11.1, 11.1 Hz, 1 H), 2.42 (ddq, J=9.7, 6.6, 6.6 Hz, 1 H), 2.10-2.00 (m, 1 H), 1.53 (s, 3 H), 1.43 (s, 3 H), 0.83 (s, 9 H), 0.81 (d, J=6.7 Hz, 3 H), 0.75 (d, J=6.8 Hz, 3 H), 0.03 (s, 3 H), -0.02 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d, 135.3 (J_(cp) =2.8 Hz), 133.3 (J_(cp) =9.9 Hz), 131.0, 130.6 (J_(cp) =12.4 Hz), 128.0, 118.2 (J_(cp) =85.6 Hz), 80.4 (J_(cp) =13.3 Hz), 36.0, 33.0 (J_(cp) =4.0 Hz), 26.1, 25.6, 25.1 (J_(cp) =50.8 Hz), 18.3, 18.1, 17.9, 16.4, -3.3, -4.0; high resolution mass spectrum (FAB, NBA) m/z 531.3221 [(M-I)⁺ ; calcd for C₃₄ H₄₈ OPSi: 531.3213].

Olefin (-)-47: Colorless oil; [α]²³ _(D) -14°©0.36, CHCl₃); IR (CHCl₃) 2960 (s), 2930 (s), 2860 (s), 1470 (m), 1460, 1370 (m), 1360 (m), 1250 (m), 1206 (w), 1165 (m), 1140 (m), 1070 (s), 1020 (s), 1000 (m), 932 (w), 908 (w), 897 (w), 853 (m), 830 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 3.63 (d, br, J=3.6 Hz, 1 H), 2.50 (apparent q, J=7.3 Hz, 1 H), 2.28 (ddd, J=15.5, 7.7, 0.8 Hz, 1 H), 2.13-2.03 (m, 1 H), 1.99-1.91 (m, 1 H), 1.60 (apparent br s, 3 H), 1.57 (apparent d, J=0.8 Hz, 1 H), 0.94 (d, J=6.7 Hz, 3 H), 0.91 (d, J=7.4 Hz, 3 H), 0.85 (s, 9 H), 0.01 (apparent s, 6 H); ¹³ C NMR (125 MHZ, CDCl₃) d 138.9 (q), 122.0 (q), 82.9, 46.1, 36.4, 35.8 (CH₂), 25.9, 21.2, 20.4, 18.3 (q), 18.0, 14.3, -4.6, -4.8; high resolution mass spectrum (CI, NH₃) m/z 269.2310 [(M+H)⁺ ; calcd for C₁₆ H₃₃ OSi: 269.2300].

Olefin (-)-48: Colorless oil; [α]²³ _(D) -3.8°©0.24, CHCl₃); IR (CHCl₃) 2953 (s), 2925 (s), 2880 (m), 2855 (m), 1638 (w), 1470 (m), 1460 (m), 1385 (w), 1373 (m), 1360 (w), 1250 (m), 1135 (m), 1117 (m), 1100 (m), 1075 (m), 1028 (m), 1000 (m), 932 (w), 865 (m), 830 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, C₆ D₆) d 4.84-4.83 (m, 1 H), 4.79-4.77 (m, 1 H), 3.46 (apparent t, J=5.3 Hz, 1 H), 1.94-1.88 (m, 1 H), 1.87-1.78 (m, 2 H), 1.73 (ddd, J=12.4, 7.3, 7.3 Hz, 1 H), 1.66 (apparent dd, J=1.3, 0.8 Hz, 3 H), 1.45 (ddd, J=12.2, 10.3, 8.7 Hz, 1 H), 1.00 (d, J=6.9 Hz, 3 H), 0.99 (s, 9 H), 0.96 (d, J=6.7 Hz, 3 H), 0.06 (s, 3 H), 0.05 (s, 3 H); ¹³ C NMR (125 MHZ, C₆ D₆) d 147.4 (q), 110.3 (CH₂), 82.3, 53.1, 45.4, 37.5 (CH₂), 37.3, 26.1, 19.3, 18.4 (q), 18.0, 15.6, -4.4, -4.5; high resolution mass spectrum (CI, NH₃) m/z 269.2315 [(M+H)⁺ ; calcd for C₁₆ H₃₃ OSi: 269.2300].

EXAMPLE 40

Alcohol (+)-51

A solution of olefin (+)-44 (70.9 mg, 0.28 mmol) in EtOH/EtOAc (1:8, 4.5 mL) was treated with Pd/C (10% wet, E101 NE/W, 15.2 mg) under H₂ atmosphere for 18 h. The mixture was then filtered through a short silica pipet and concentrated. Flash chromatography (5% ethyl acetate/hexane) provided (+)-51 (70.8 mg, 100% yield) as a colorless oil. [α]²³ _(D) +28°©0.15, CHCl₃); IR (CHCl₃) 3680 (w), 3620 (w), 3500 (w, br), 3010 (m), 2960 (s), 2935 (s), 2900 (m), 2885 (m), 2860 (m), 1522 (w), 1510 (w), 1470 (m), 1426 (m), 1420 (m), 1412 (m), 1387 (m), 1370 (m), 1255 (m), 1205 (m), 1070 (m), 1030 (m), 1013 (m) 1002 (m), 980 (m), 925 (m), 833 (s), 720 (m), 665 (m), 658 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 3.60-3.56 (m, 2 H), 3.46 (dd, J=5.5, 3.8 Hz, 1 H), 2.46 (br s, 1 H), 1.89-1.81 (m, 1 H), 1.74-1.66 (m, 1 H), 1.64-1.56 (m, 1 H), 1.21 (ddd, J=13.3, 8.9, 4.6 Hz, 1 H), 1.09 (ddd, J=13.7, 9.6, 5.3 Hz, 1 H), 0.94 (d, J=7.0 Hz, 3 H), 0.90 (s, 9 H), 0.88 (d, J=6.6 Hz, 3 H), 0.86 (d, J=6.9 Hz, 3 H), 0.83 (d, J=6.6 Hz, 3 H), 0.095 (s, 3 H), 0. 07 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 81.3, 66.3, 42.5, 37.8, 35.7, 26.1, 25.4, 23.8, 21.8, 16.4, 15.1, -3.9, -4.1; high resolution mass spectrum (CI, NH₃) m/z 289.2565 [(M+H)⁺ ; calcd for C₁₆ H₃₇ O₂ Si: 289.2562].

EXAMPLE 41

Iodide (+)-52

A solution of alcohol (+)-51 (150 mg, 0.520 mmol), PPh₃ (205 mg, 0.780 mmol) and imidazole (53 mg, 0.780 mmol) in benzene/ether (1:2; 6.0 mL) was treated with iodine (198 mg, 0.780 mmol) under vigorous stirring at room temperature. After 40 min, the mixture was diluted with ether (100 mL), washed with saturated Na₂ S₂ O₃ (50 mL), brine (100 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (hexane) provided (+)-51 (195 mg, 94% yield) as a colorless oil: [α]²³ _(D) +24.2°©2.21, CHCl₃); IR (CHCl₃) 2960 (s), 2935 (s), 2900 (m), 2860 (s), 1470 (m), 1463 (m), 1425 (w), 1405 (w), 1382 (m), 1368 (m), 1360 (m), 1290 (w), 1255 (s), 1190 (m), 1170 (m), 1082 (s), 1065 (m), 1028 (m), 1003 (m), 970 (w), 932 (w), 832 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 3.41 (dd, J=9.6, 3.7 Hz, 1 H), 3.38 (dd, J=6.3, 2.6 Hz, 1 H), 3.10 (dd, J=9.6, 7.5 Hz, 1 H), 1.72-1.56 (m, 3 H), 1.17 (ddd, J=13.4, 8.3, 5.4 Hz, 1 H), 1.09 (ddd, J=13.3, 5.9, 2.1 Hz, 1 H), 0.99 (d, J=6.8 Hz, 3 H), 0.89 (s, 9 H), 0.88 (d, J=6.6 Hz, 3 H), 0.84 (d, J=6.6 Hz, 3 H), 0.81 (d, J=6.8 Hz, 3 H), 0.09 (s, 3 H), 0.06 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 79.1, 43.7, 39.8, 33.8, 26.2, 25.3, 23.5, 22.0, 18.7, 18.5, 15.9, 14.4, -3.65, -3.71; high resolution mass spectrum (CI, NH₃) m/z 399.1572 [(M+H)⁺ ; calcd for C₁₆ H₃₆ OISi: 399.1580].

EXAMPLE 42

Wittig Reagent (+)-53

A mixture of Iodide (+)-52 (195 mg, 0.489 mmol) and benzene (100 mL) was treated with I--Pr₂ NEt (85 μL, 0.488 mmol) and PPh₃ (1.28 g, 4.88 mmol), then heated at 70° C. for 24 h. 10 The mixture was extracted with hexane (3×20 mL). The residue was purified by flash chromatography (3% MeOH/CHCl₃) furnishing (+)-53 (303 mg, 94% yield) as a white foam; [α]²³ _(D) =3.3°©2.14, CHCl₃); IR (CHCl₃) 2950 (s), 2930 (s), 2855 (m), 1588 (w), 1482 (w), 1463 (m), 1438 (s), 1385 (m), 1365 (w), 1253 (m), 1225 15 (m), 1207 (m), 1110 (s), 1080 (m), 1032 (m), 1000 (m), 832 (s), 804 (m), 708 (m), 680 (m), 653 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.83-7.67 (m, 15 H), 3.70 (ddd, J=15.6, 11.0, 11.0 Hz, 1 H), 3.52 (dd, J=7.6, 1.7 Hz, 1 H), 3.45 (apparent t, J=15.4 Hz, 1 H), 2.08-1.97 (m, 1 H), 1.70-1.62 (m, 1 H), 1.51 (9 20 lines, J=6.5 Hz, 1 H), 1.09-0.97 (m, 2 H), 0.850 (s, 9 H), 0.79 (d, J=6.7 Hz, 3 H), 0.77 (d, J=7.9 Hz, 3 H), 0.74 (d, J=6.5 Hz, 3 H), 0.68 (d, J=6.8 Hz, 3 H), 0.12 (s, 3 H), 0.11 (s, 3 H); 13C NMR (125 MHZ, CDCl₃) d 135.2 (J_(cp) =2.7 Hz), 133.6 (J_(cp) =9.9 Hz), 130.6 (J_(cp) =12.4 Hz), 118.5 (J_(cp) =85.5 25 Hz), 80.1 (J_(cp) =12.9 Hz), 43.5, 33.6, 32.6 (J_(cp) =3.7 Hz), 26.2, 25.3 (J_(cp) =51.1 Hz), 25.0, 23.4, 21.7, 18.6, 18.5, 13.7, -2.7, -3.8; high resolution mass spectrum (FAB,NBA) m/z 533.3369 [(M-I)⁺ ; calcd for C₃₄ H₅₀ OPSi: 533.3357].

EXAMPLE 43

Olefin (-)-54

Phosphonium salt (-)-49 was dried azeotropically with anhydrous benzene and heated at 50° C. under vacuum for 3 h before use. A solution of (-)-49 (97.7 mg, 0.0917 mmol) in THF (700 pL) was cooled to -78° C. and treated with NaHMDS (1.0 M in THF, 85.5 μL, 0.0855 mmol). The mixture was stirred for 20 min at 0° C., recooled to -78° C. and aldehyde C (28.0 mg, 0.0570 mmol) in THF (300 pL) was added. After 10 min at -78° C. and 2 h at room temperature, the mixture was quenched with saturated aqueous NH₄ Cl (1.0 mL) and extracted with ether (30 mL). The ether solution was washed with water, brine (30 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (2% ethyl acetate/hexane) provided (-)-56 (50.0 mg, 76% yield) as a colorless oil: [α]²³ _(D) -44.9°©2.09, CHCl₃); IR (CHCl₃) 2960 (s), 2930 (s), 2855 (s), 1615 (m), 1587 (w), 1517 (m), 1463 (s), 1380 (m), 1360 (m), 1320 (m), 1300 (m), 1250 (s), 1170 (m), 1160 (m), 1120-1000 (s, br), 990 (m), 965 (m), 935 (m), 900 (m), 835 (s), 807 (m), 670 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.35 (d, J=8.7 Hz, 2 H), 6.85 (d, J=8.8 Hz, 2 H), 5.37 (s, 1 H), 5.27 (dd, J=11.2, 7.8 Hz, 1 H), 5.19 (apparent t, J=10.9 Hz, 1 H), 5.08 (d, J=10.1 Hz, 1 H), 5.06 (d, J=2.2 Hz, 1 H), 4.68 (apparent t, J=9.1 Hz, 1 H), 4.08 (dd, J=11.2, 4.7 Hz, 1 H), 3.78 (s, 3 H), 3.68 (apparent t, J=10.1 Hz, 1 H), 3.61 (dd, J=7.1, 1.7 Hz, 1 H), 3.53 (apparent t, J=2.6 Hz, 1 H), 3.50 (dd, J=9.9, 1.6 Hz, 1 H), 3.46 (apparent t, J=11.1 Hz, 1 H), 3.25 (apparent t, J=5.3 Hz, 1 H), 2.71-2.58 (m, 1 H), 2.68 (dq, J=12.8, 7.4 Hz, 1 H), 2.62 (dq, J=12.8, 7.4 Hz, 1 H), 2.50 (m, 1 H), 2.30 (apparent t, J=12.2 Hz, 1 H), 2.08-2.01 (m, 1 H), 1.98-1.90 (m, 1 H), 1.88 (dqd, J=7.1, 7.1, 1.7 Hz, 1 H), 1.82 (apparent qt, J=7.1, 2.6 Hz, 1 H), 1.65 (br d, J=12.4 Hz, 1 H), 1.62-1.57 (m, 2 H), 1.56 (d, J=0.4 Hz, 3 H), 1.38 (ddd, J=13.6, 10.7, 1.5 Hz, 1 H), 1.29-1.22 (apparent t, J=7.4 Hz, 3 H), 1.00 (d, J=7.1 Hz, 3 H), 0.94 (d, J=7.3 Hz, 3 H), 0.930 (d, J=6.9 Hz, 3 H), 0.925 (d, J=7.1 Hz, 3 H), 0.90 (s, 18 H), 0.89 (s, 9 H), 0.86 (s, 9 H), 0.74 (apparent d, J=6.6 Hz, 6 H), 0.73 (d, J=6.1 Hz, 3 H), 0.05 (s, 3 H), 0.04 (s, 3 H), 0.03 (s, 3 H), 0.019 (s, 3 H), 0.017 (s, 3 H), 0.013 (s, 3 H), 0.009 (s, 3 H), 0.00 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.8, 134.4, 131.9, 131.8, 131.5, 131.4, 127.3, 113.4, 101.0, 83.4, 80.9, 80.4, 78.5, 76.7, 76.5, 74.2, 73.3, 65.5, 55.2, 42.5, 41.9, 38.2, 37.5, 37.1, 35.4, 34.4, 33.8, 26.3, 26.2, 26.0, 25.9, 25.1, 23.2, 18.5, 18.4, 18.12, 18.08, 17.0, 16.6, 15.6, 14.4, 12.7, 12.1, 11.6, 10.9, -2.7, -3.5, -3.66, -3.69, -4.2, -4.5, -4.9, -5.0; high resolution mass spectrum (FAB, NBA) m/z 1171.7799 [(M+Na)⁺ ; calcd for C₆₃ H₁₂₀ O₈ SSi₄ Na: 1171.7781].

EXAMPLE 44

Hydroxy Diene (-)-55

A solution of the olefin (-)-54 (49.8 mg, 0.0434 mmol) in CH₂ Cl₂ (4.4 mL) was cooled to -78° C. and DIBAL (1.0 M in toluene, 430 μL, 0.430 mmol) was added over 5 min. After 10 min at -78° C. and 30 min at 0° C., the reaction was quenched with saturated aqueous Rochelle's salt (500 μL). The mixture was diluted with ether (60 mL), washed with saturated aqueous Rochelle salt, brine (30 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (5% ethyl acetate/hexane) furnished (-)-57 (38.0 mg, 88% yield) as a colorless oil: [α]²³ _(D) -32°©1.90, CHCl₃); IR (CHCl₃) 3500 (w, br), 2960 (s), 2935 (s), 2900 (m), 2885 (m), 2860 (s), 1610 (m), 1585 (w), 1510 (m), 1470 (m), 1460 (m), 1400 (m), 1375 (m), 1360 (m), 1300 (m), 1250 (s), 1170 (m), 1095 (m), 1080 (m), 1047 (s), 1000 (m), 960 (m), 950 (m), 933 (m), 835 (s), 805 (m) , 665 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.24 (d, J=8.6 Hz, 2 H), 6.85 (d, J=8.6 Hz, 2 H), 5.27 (dd, J=11.4, 7.8 Hz, 1 H), 5.20 (apparent t, J=10.3 Hz, 1 H), 5.10 (d, J=10.0 Hz, 1 H), 5.05 (d, J=2.2 Hz, 1 H), 4.68 (apparent t, J=9.2 Hz, 1 H), 4.49 (ABq, J_(AB) =10.4 Hz, Δδ_(AB) =23.4 Hz, 2 H), 3.78 (s, 3 H), 3.73 (ddd, J=10.7, 4.0, 4.0 Hz, 1 H), 3.68 (apparent t, J=10.4 Hz, 1 H), 3.57 (ddd, J=10.6, 5.1, 5.1 Hz, 1 H), 3.53 (dd, J=5.4, 3.4 Hz, 1 H), 3.50 (apparent t, J=5.2 Hz, 1 H), 3.35 (apparent t, J=5.5 Hz, 1 H), 3.26 (apparent t, J=5.2 Hz, 1 H), 2.68 (dq, J=12.8, 7.4 Hz, 1 H), 2.61 (dq, J=12.8, 7.5 Hz, 1 H), 2.71-2.58 (m, 2 H), 2.51-2.44 (m, 1 H), 2.22 (apparent t, J=12.4 Hz, 1 H), 1.99-1.86 (m, 3 H), 1.81 (apparent qt, J=7.1, 2.6 Hz, 1 H), 1.72 (br d, J=12.7 Hz, 1 H), 1.62-1.57 (m, 1 H), 1.61 (s, 3 H), 1.56-1.48 (m, 1 H), 1.38 (ddd, J=13.5, 12.3, 1.4 Hz, 1 H), 1.27 (apparent t, J=7.4 Hz, 3 H), 1.03 (d, J=6.9 Hz, 3 H), 1.02 (d, J=6.8 Hz, 3 H), 0.95-0.92 (m, 9 H), 0.93 (s, 9 H), 0.90 (s, 9 H), 0.89 (s, 9 H), 0.86 (s, 9 H), 0.74 (d, J=8.0 Hz, 3 H), 0.73 (d, J=7.0 Hz, 3 H), 0.08 (s, 6 H), 0.05 (s, 3 H), 0.024 (s, 3 H), 0.020 (s, 3 H), 0.012 (s, 3 H), 0.009 (s, 3 H), 0.006 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.4, 134.4, 132.3, 131.7, 130.9, 130.4, 129.3, 114.0, 86.3, 80.9, 80.4, 77.6, 76.5, 75.3, 74.2, 65.6, 65.5, 55.3, 42.6, 41.9, 40.0, 37.6, 37.0, 36.8, 35.9, 35.2, 34.5, 26.30, 26.27, 25.9, 25.8, 25.1, 23.2, 18.53, 18.47, 18.13, 18.07, 17.1, 16.6, 15.7, 15.6, 14.4, 13.6, 11.6, 11.4, -2.8, -3.2, -3.4, -3.6, -4.2, -4.5, -4.9; high resolution mass spectrum (FAB, NBA) m/z 1173.7859 [(M+Na)⁺ ; calcd for C₆₃ H₁₂₂ O₈ SSi₄ Na: 1173.7835].

EXAMPLE 45

Aldehyde (-)-56

A solution of alcohol (-)-55 (13.8 mg, 0.0120 mmol) and Et₃ N (42 μL, 0.30 mmol) in CH₂ Cl₂ (200 μL) was cooled to 0° C. and treated with SO₃.pyridine (40 mg, 0.251 mmol) in DMSO (600 μL). After 45 min at 0° C., the mixture was diluted with ethyl acetate (30 mL), washed with aqueous NaHSO₄ (1.0 M, 30 mL), brine (2×30 mL), dried over MgSO₄, filtered and concentrated. Pipette flash chromatography (3% ethyl acetate/hexane) afforded (-)-56 (13.2 mg, 96% yield) as a colorless oil: [α]²³ _(D) -32.1°©1.40, CHCl₃); IR (CHCl₃) 2960 (s), 2935 (s), 2880 (m), 1720 (m), 1610 (m), 1512 (m), 1470 (m), 1460 (m), 1387 (m), 1380 (m), 1360 (m), 1340 (m), 1320 (m), 1300 (m), 1250 (s), 1110 (s), 1098 (s), 1080 (s), 1048 (s), 1002 (m), 988 (m), 965 (m), 950 (m), 935 (m), 835 (s) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 9.78 (d, J=2.5 Hz, 1 H), 7.20 (d, J=8.6 Hz, 2 H), 6.85 (d, J=8.7 Hz, 2 H), 5.27 (dd, J=11.1, 7.8 Hz, 1 H), 5.19 (apparent t, J=10.4 Hz, 1 H), 5.10 (d, J=10.0 Hz, 1 H), 5.05 (d, J=2.1 Hz, 1 H), 4.67 (apparent t, J=8.9 Hz, 1 H), 4.45 (apparent s, 2 H), 3.78 (s, 3 H), 3.68 (apparent t, J=10.2 Hz, 1 H), 3.58-3.56 (m, 2 H), 3.51 (apparent t, J=2.6 Hz, 1 H), 3.25 (apparent t, J=5.2 Hz, 1 H), 2.73 (dqd, J=7.1, 6.0, 2.6 Hz, 1 H), 2.70-2.57 (m, 3 H), 2.51-2.44 (m, 1 H), 2.23 (apparent t, J=12.4 Hz, 1 H), 1.98-1.85 (m, 2 H), 1.81 (apparent qt, J=7.1, 2.6 Hz, 1 H), 1.67 (br d, J=13.0 Hz, 1 H), 1.60 (s, 3 H), 1. 62-1.50 (m, 2H), 1.37 (ddd, J=13.8, 10.4, 1.5 Hz, 1 H), 1.26 (apparent t, J=7.4 Hz, 3 H), 1.10 (d, J=7.0 Hz, 3 H), 1.02 (d, J=7.0 Hz, 3 H), 0. 938 (d, J=7.1 Hz, 3 H), 0. 932 (d, J=7.8 Hz, 3 H), 0.919 (s, 9 H), 0.918 (d, J=6.6 Hz, 3 H), 0.90 (s, 9 H), 0.88 (s, 9 H), 0. 86 (s, 9 H), 0.732 (d, J=6.7 Hz, 3 H), 0.726 (d, J=6.8 Hz, 3 H), 0.07 (s, 3 H), 0.053 (s, 3 H), 0.047 (s, 3 H), 0.02 (s, 6 H), 0.009 (s, 3 H), 0.005 (s, 6 H); ¹³ C NMR (125 MHZ, CDCl₃) d 204.6, 159.3, 134.4, 132.3, 131.8, 130.8, 130.3, 129.1, 128.3, 113.8, 82.6, 80.9, 80.4, 76.5, 74.5, 74.2, 65.5, 55.3, 49.5, 42.5, 41.9, 40.3, 37.1, 36.8, 35.4, 34.9, 34.4, 26.3, 26.2, 25.9, 25.8, 25.1, 23.2, 18.49, 18.45, 18.12, 18.07, 17.0, 16.6, 15.6, 14.4, 13.3, 12.1, 11.6, 11.4, -2.8, -3.3, -3.4, -3.7, -4.2, -4.5, -4.9, -5.0; high resolution mass spectrum (FAB, NBA) m/z 1171.7670 [(M+Na)⁺ ; calcd for C₆₃ H₁₂₀ O₈ SSiNa: 1171.7676].

EXAMPLE 46

Tetraene (-)-57

A solution of Ph₂ PCH₂ CH=CH₂ (40 μL, 0.19 mmol) in THF (1.0 mL) was cooled to -78° C. and t-BuLi (1.7 M in pentane, 72.0 pL, 0.122 mmol) was added. The mixture was stirred at 0° C. for 30 min, recooled to -78° C. and treated with Ti(OiPr)₄ (45 μL, 0.15 mmol). After 30 min, a cold (-78° C.) solution of the aldehyde (-)-56 (30.2 mg, 0.0262 mmol) in THF (1.0 mL) was introduced via cannula, and the resultant mixture was stirred for 10 min at -78° C. and 1 h at 0° C. MeI (20 μL, 0.32 mmol) was then added, and the reaction was maintained at 0° C. for 30 min, warmed to room temperature, protected from light with aluminum foil, and stirred overnight. The reaction mixture was diluted with ether (30 mL), washed with aqueous NaHSO₄ (1.0 M), brine (30 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (2% ethyl acetate/hexane) gave a 16:1 mixture of Z/E isomers (20.0 mg, 70% yield) as an oil. Pipette flash chromatography (20% benzene/hexane) furnished the Z-olefin (-)-57 as a colorless oil: [α]²³ _(D) -57.2°©2.56, CHCl₃); IR (CHCl₃) 3015 (m), 2960 (s), 2940 (s), 2900 (m), 2885 (m), 2860 (s), 1613 (w), 1515 (m), 1475 (m), 1465 (m), 1390 (w), 1380 (w), 1360 (w), 1250 (s), 1110 (m), 1100 (m), 1080 (m), 1050 (s), 1003 (m), 963 (w), 950 (w), 835 (s), 800 (m), 790 (m), 770 (m), 700 (w), 690 (w), 670 (w), 655 (w) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.25 (d, J=8.2 Hz, 2 H), 6.84 (d, J=8.7 Hz, 2 H), 6.57 (dddd, J=16.8, 11.0, 11.0, 0.7 Hz, 1 H), 6.00 (apparent t, J=11.1 Hz, 1 H), 5.55 (apparent t, J=10.5 Hz, 1 H), 5.26 (dd, J=11.2, 7.8 Hz, 1 H), 5.20-5.16 (m, 2 H), 5.09 (d, J=10.1 Hz, 1 H), 5.05 (d, J=2.2 Hz, 1 H), 5.03 (d, J=10.0 Hz, 1 H), 4.67 (apparent t, J=9.1 Hz, 1 H), 4.49 (ABq, J_(AB) =10. 6 Hz, Δδ_(AB) =41.3 Hz, 2 H), 3.78 (s, 3 H), 3.68 (apparent t, J=10.2 Hz, 1 H), 3.52 (apparent t, J=2.6 Hz, 1 H), 3.43 (dd, J=4.8, 3.9 Hz, 1 H), 3.24-3.21 (m, 2 H), 3.01-2.94 (m, 1 H), 2.67 (dq, J=12.8, 7.4 Hz, 1 H), 2.61 (dq, J=12.8, 7.5 Hz, 1 H), 2.71-2.57 (m, 1 H), 2.46-2.39 (m, 1 H), 2.00 (apparent t, J=12.4 Hz, 1 H), 1.83-1.73 (m, 3 H), 1.64 (br d, J=14.0 Hz, 1 H), 1.62-1.52 (m, 2 H), 1.55 (d, J=0.5 Hz, 3 H), 1.36 (ddd, J=13.7, 10.8, 1.5 Hz, 1 H), 1.26 (d, J=7.4 Hz, 3 H), 1.25 (d, J=7.4 Hz, 3 H), 1.08 (d, J=6.8 Hz, 3 H), 0.98 (d, J=6.8 Hz, 3 H), 0.94 (d, J=7.1 Hz, 3 H), 0.93 (s, 9 H), 0.90 (s, 9 H), 0.89 (s, 9 H), 0.89-0.86 (m, 3 H), 0.86 (s, 9 H), 0.73 (d, J=6.8 Hz, 3 H), 0.70 (d, J=6.7 Hz, 3 H), 0.08 (s, 6 H), 0.05 (s, 3 H), 0.02 (s, 3 H), 0.013 (s, 3 H), 0.010 (s, 6 H), -0.02 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.1, 134.5, 134.3, 132.2, 131.9, 131.8, 131.2, 129.13, 129.07, 117.6, 113.7, 84.6, 80.9, 80.5, 76.5, 75.0, 74.2, 65.5, 55.3, 42.5, 41.9, 40.2, 37.2, 36.1, 35.4, 35.3, 34.5, 29.7, 26.3, 26.0, 25.9, 25.1, 23.1, 18.7, 18.6, 18.5, 18.14, 18.09, 17.0, 16.8, 15.6, 14.8, 14.4, 11.6, 10.6, -2.8, -3.2, -3.3, -3.6, -4.2, -4.5, -4.90, -4.93; high resolution mass spectrum (FAB, NBA) m/z 1195.8001 [(M+Na)⁺ ; calcd for C₆₆ H₁₂₄ O₇ SSi₄ Na: 1195.8042].

EXAMPLE 47

Lactone (-)-58

A solution of diene (-)-57 (7.0 mg, 0.00597 mmol) in THF/CH₃ CN (2:1, 1.50 mL) was treated with pH 7.0 phosphate buffer (500 μL) and HgCl₂ (215 mg). The suspension was stirred at room temperature for 40 min, diluted with ether (30 mL), washed with brine (2×30 mL), dried over MgSO₄, filtered and concentrated. Pipette flash chromatography (5% ethyl acetate/hexane) provided a mixture of lactols as a colorless oil which was further treated with DMSO (1.0 mL) and Ac₂ O (200 mL) at room temperature for 2 days. The mixture was diluted with ether (30 mL), washed with saturated NaHCO₃ (30 mL), brine (30 mL), dried over MgSO₄, filtered and concentrated. Pipette flash chromatography (2% ethyl acetate/hexane) provided (-)-58 (5.5 mg, 82% yield from (-)-57) as a colorless oil: [α]²³ _(D) -31.6°©0.23, CHCl₃); IR (CHCl₃) 3015 (m), 2960 (s), 2930 (s), 2880 (m), 2855 (m), 1725 (m), 1610 (w), 1510 (w), 1460 (m),1385 (m), 1373 (m), 1360 (m), 1300 (w), 1250 (s), 1230 (m), 1200 (m), 1170 (m), 1120 (m), 1097 (m), 1060 (m), 1045 (s), 1020 (m), 1003 (m), 980 (w), 955 (w), 930 (w), 905 (w), 867 (m), 835 (s), 800 (m), 695 (m), 670 (m), 660 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 7.25 (d, J=9.0 Hz, 2 H), 6.84 (d, J=8.7 Hz, 2 H), 6.57 (ddd, J=16.7, 10.6, 10.6 Hz, 1 H), 6.00 (apparent t, J=11.0 Hz, 1 H), 5.55 (apparent t, J=10.5 Hz, 1 H), 5.26 (dd, J=11.1, 7.9 Hz, 1 H), 5.19 (dd, J=15.4, 1.4 Hz, 1 H), 5.18 (apparent t J=10.1 Hz, 1 H), 5.10 (d, J=10.2 Hz, 1 H), 5.01 (d, J=10.0 Hz, 1 H), 4.75 (apparent t, J=9.2 Hz, 1 H), 4.50 (ddd, J=10.5, 1.3, 1.3 Hz, 1 H), 4.50 (ABq, J_(AB) =10.6 Hz, Δδ_(AB) =42.6 Hz, 2 H), 3.78 (s, 3 H), 3.60 (apparent t, J=2.4 Hz, 1 H), 3.42 (dd, J=5.1, 3.7 Hz, 1 H), 3.23 (dd, J=7.5, 3.7 Hz, 1 H), 3.20 (apparent t, J=5.4 Hz, 1 H), 3.01-2.94 (m, 1 H), 2.60 (qd, J=7.7, 2.6 Hz, 1 H), 2.62-2.55 (m, 1 H), 2.45-2.38 (m, 1 H), 1.98 (apparent t, J=12.3 Hz, 1 H), 1.84-1.67 (m, 3 H), 1.63 (br d, J=13.2 Hz, 1H), 1.52 (s, 3 H), 1.55-1.48 (m, 1 H), 1.20 (d, J=7.6 Hz, 3 H), 1.09 (d, J=6.8 Hz, 3 H), 0.98 (d, J=6.8 Hz, 3 H), 0. 93 (apparent d, J=6.7 Hz, 6 H), 0.93 (s, 9 H), 0.89 (s, 9 H), 0.86 (s, 9 H), 0.85 (s, 9 H), 0.84 (d, J=6.8 Hz, 3 H), 0.69 (d, J=6.7 Hz, 3 H), 0.085 (s, 3 H), 0.079 (s, 3 H), 0.051 (s, 3 H), 0.046 (s, 3 H), 0.042 (s, 3 H), 0.029 (s, 3 H), 0.028 (s, 3 H), -0.02 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 173.2, 159.1, 134.4, 133.4, 132.4, 132.2, 131.9., 131.3, 131.2, 129.11, 129.09, 117.6, 113.7, 84.6, 80.5, 76.9, 75.0, 74.9, 64.6, 55.3, 44.1, 42.7, 40.1, 37.5, 36.0, 35.44, 35.37, 35.2, 34.2, 26.31, 26.28, 25.9, 25.7, 23.0, 18.7, 18.6, 18.4, 18.1, 18.0, 17.1, 16.5, 16.4, 14.9, 14.1, 10.5, -3.0, -3.2, -3.3, -4.3, -4.4, -4.5, -4.8 4.9; high resolution mass spectrum (FAB, NBA) m/z 1149.7836 [(M+Na)⁺ ; Calcd for C₆₄ H₁₁₈ O₈ Si₄ Na: 1149.7802].

EXAMPLE 48

Alcohol (-)-59

A solution of (-)-58 (4.0 mg, 0.00355 mmol) in CH₂ Cl₂ (500 μL) was treated with H₂ O (50 μL) and DDQ (3.0 mg, 0.0132 mmol) at 0° C. After 1 h, the mixture was diluted with ethyl acetate (30 mL), washed with brine (3×30 mL), dried over MgSO₄, filtered and concentrated. Pipette flash chromatography (2% ethyl acetate/hexane) provided (-)-59 (3.4 mg, 95% yield) as a colorless oil: [α]²³ _(D) -20°©0.34, CHCl₃); IR (film, CHCl₃ on NaCl plate) 3500 (w, br), 2960 (s), 2930 (s), 2890 (s), 2855 (s), 1740 (m), 1460 (m), 1405 (m), 1380 (m), 1360 (s), 1253 (m), 1220 (m), 1120 (s), 1093 (s), 1075 (s), 1045 (s), 1022 (s), 1002 (m), 980 (m), 933 (m), 902 (m), 833 (s), 808 (m), 770 (s), 663 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 6.61 (ddd, J=16.8, 10.9, 10.9 Hz, 1 H), 6.13 (apparent t, J=11.0 Hz, 1 H), 5.32 (apparent t, J=10.5 Hz, 1 H), 5.28 (dd, J=11.1, 7.9 Hz, 1 H), 5.24-5.21 (m, 1 H), 5.19 (apparent t, J=10.3 Hz, 1 H), 5.14 (d, J=10.2 Hz, 1 H), 5.06 (d, J=10.0 Hz, 1 H), 4.76 (apparent t, J 9.3 Hz, 1 H), 4.50 (apparent t, J=9.9 Hz, 1 H), 3.62 (apparent t, J=2.4 Hz, 1 H), 3.60 (dd, J=5.5, 3.4 Hz, 1 H), 3.32 (br d, J=5.3 Hz, 1 H), 3.24 (apparent t, J=5.1 Hz, 1 H), 2.79 (ddq, J=9.9, 6.7, 6.7 Hz, 1 H), 2.60 (qd, J=7.6, 2.7 Hz, 1 H), 2.63-2.57 (m, 1 H), 2.50-2.45 (m, 1 H), 2.16 (apparent t, J=12.3 Hz, 1 H), 1.90-1.77 (m, 3 H), 1.75-1.69 (m, 2 H), 1.57 (s, 3 H), 1.60-1.50 (m, 1 H), 1.20 (d, J=7.6 Hz, 3 H), 0.96 (d, J=6.8 Hz, 3 H), 0.95 (d, J=6.6 Hz, 3 H), 0.95-0.93 (m, 6 H), 0.91 (s, 9 H), 0.89 (s, 9 H), 0.89-0.84 (m, 3 H), 0.87 (s, 9 H), 0.85 (s, 9 H), 0.73 (d, J=6.8 Hz, 3 H), 0.07 (apparent s, 6 H), 0.052 (s, 3 H), 0.051 (s, 3 H), 0.04 (apparent s, 6 H), 0.03 (s, 3 H), -0.01 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 173.3, 134.7, 133.5, 132.5, 132.1, 132.0, 131.5, 131.0, 118.4, 80.5, 78.8, 76.4, 74.9, 64.7, 44.1, 42.7, 38.0, 37.4, 36.3, 36.1, 35.2, 35.1, 34.2, 30 26.3, 26.2, 25.9, 25.7, 23.2, 18.5, 18.1, 18.0, 17.3, 17.2, 16.4, 16.1, 14.1, 13.7, 9.4, -3.0, -3.3, -3.6, -4.34, -4.36, -4.5, -4.8; high resolution mass spectrum (FAB, NBA) m/z 1029.7273 [(M+Na)⁺ ; calcd for C₅₆ H₁₁₀ O₇ Si₄ Na: 1029.7226].

EXAMPLE 49

Carbamate (-)-60

A solution of alcohol (-)-59 (2.2 mg, 0.00219 mmol) in CH₂ Cl₂ (500 μL) was treated with Cl₃ CON═C═O (20 μL, 0.168 mmol) at room temperature. After 30 min, the mixture was diluted with regular CH₂ Cl₂ (2.0 mL) and treated with neutral Al₂ O₃ (500 mg). The mixture was stirred at room temperature for 2 h, filtered through a short silica plug, and concentrated. Pipette flash chromatography (10% ethyl acetate/hexane) provided (-)-60 (1.9 mg, 83% yield) as a colorless oil: [α]²³ _(D) -37°©0.19, CHCl₃); IR (film, CHCl₃ on NaCl plate) 3510 (m), 3360 (m, br), 3180 (m), 2960 (s), 2930 (s), 2880 (s), 2855 (s), 1730 (s, br), 1596 (m), 1460 (s), 1385 (s), 1362 (s), 1325 (m), 1255 (s), 1220 (m), 1100 (s), 1043 (s), 983 (m), 937 (m), 904 (m), 832 (s), 770 (s), 663 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 6.58 (dddd, J=16.8, 10.6, 10.6, 0.7 Hz, 1 H), 6.01 (apparent t, J=11.0 Hz, 1 H), 5.36 (apparent t, J=10.4 Hz, 1 H), 5.27 (dd, J=11.1, 7.9 Hz, 1 H), 5.22-5.16 (m, 2 H), 5.12 (d, J=10.1 Hz, 1 H), 5.03 (d, J=10.0 Hz, 1 H), 4.76 (apparent t, J=9.2 Hz, 1 H), 4.71 (apparent t, J=6.1 Hz, 1 H), 4.50 (ddd, J=10.5, 10.5, 1.3 Hz, 1 H), 4.44 (br s, 2 H), 3.62 (apparent t, J=2.4 Hz, 1 H), 3.42 (apparent t, J=4.5 Hz, 1 H), 3.22 (apparent t, J=5.3 Hz, 1 H), 2.98 (ddq, J=10.1, 6.6, 6.6 Hz, 1 H), 2.60 (qd, J=7.6, 2.7 Hz, 1 H), 2.63-2.55 (m, 1 H), 2.48-2.41 (m, 1 H), 2.09 (apparent t, J=12.4 Hz, 1 H), 1.93-1.88 (m, 1 H), 1.87-1.77 (m, 2 H), 1.71 (ddd, J=14.1, 10.8, 1.6 Hz, 1 H), 1.67 (br d, J=13.7 Hz, 1 H), 1.56 (apparent s, 3 H), 1.55-1.50 (m, 1 H), 1.21 (d, J=7.6 Hz, 3 H), 0.98 (d, J=6.8 Hz, 3 H), 0.95 (d, J=7.0 Hz, 3 H), 0.94 (d, J=7.5 Hz, 3 H), 0.918 (d, J=6.8 Hz, 3 H), 0.915 (s, 9 H), 0.89 (s, 9 H), 0.86 (s, 9 H), 0.853 (d, J=6.4 Hz, 3 H), 0.847 (s, 9 H), 0.70 (d, J=6.8 Hz, 3 H), 0.09 (s, 3 H), 0.07 (s, 3 H), 0.053 (s, 3 H), 0.051 (s, 3 H), 0.040 (s, 3 H), 0.037 (s, 3 H), 0.03 (s, 3 H), -0.02 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 173.3, 156.9, 133.6, 133.5, 132.4, 132.1, 131.9, 131.4, 129.8,118.0, 80.5, 78.9, 74.9, 64.6, 44.2, 42.7, 37.8, 37.4, 36.0, 35.3, 35.2, 34.5, 34.2, 26.3, 26.2, 25.9, 25.7, 23.0, 18.5, 18.4, 18.1, 18.0, 17.5, 17.1, 16.44, 16.38, 14.1, 13.7, 10.1, -3.0, -3.4, -3.6, -4.4, -4.5, -4.8; high resolution mass spectrum (FAB, NBA) m/z 1072.7264 [(M+Na)⁺ ; calcd for C₅₇ H₁₁₁ NO₈ Si₄ Na: 1072.7283].

EXAMPLE 50

Discodermolide [(-)-1].

A solution of olefin (-)-60 (5.8 mg, 5.5 mmol) in 48% HF--CH₃ CN (1:9, 1.0 mL) was stirred at room temperature for 12 h, then quenched with saturated aqueous NaHCO₃ (5.0 mL). The mixture was extracted with ethyl acetate (3×10 mL). The combined organic extracts were washed with brine (5.0 mL), dried over MgSO₄, filtered and concentrated. Pipette flash chromatography (gradient elution, 1:30 to 1:6 MeOH/CHCl₃) provided (-)-1 (2.0 mg, 60% yield) as a white amorphous solid: [α]²³ _(D) -16°©0.03, MeOH); IR (CHCl₃) 3690 (w), 3620 (w), 3540 (w), 3430 (w), 3020 (s), 2975 (m), 2935 (m), 1740 (m), 1590 (w), 1540 (w), 1520 (w), 1467 (w), 1430 (w), 1385 (m), 1330 (w), 1233 (s), 1210 (s), 1100 (w), 1045 (m), 1033 (m), 975 (w), 930 (m), 910 (w), 793 (m), 777 (m), 765 (m), 750 (m), 705 (m), 687 (m), 670 (m), 660 (m), 625 (w) cm^(-l) ; ¹ H NMR (500 MHZ, CDCl₃) d 6.60 (dddd, J=16.8, 8.4, 8.4, 0.8 Hz, 1 H), 6.02 (apparent t, J=11.1 Hz, 1 H), 5.51 (dd, J=11.2, 7.9 Hz, 1 H), 5.42 (ddd, J=10.6, 10.6, 0.6 Hz, 1 H), 5.34 (apparent t, J=10.4 Hz, 1 H), 5.20 (dd, J=16.9, 1.9 Hz, 1 H), 5.16 (d, J=10.0 Hz, 1 H), 5.11 (d, J=10.1 Hz, 1 H), 4.77-4.69 (m, 1 H), 4.70 (dd, J=7.3, 4.2 Hz, 1 H), 4.60 (ddd, J=10.0, 10.0, 2.4 Hz, 1 H), 4.56 (br s, 2 H), 3.73 (m, 1 H), 3.28 (m, 1 H), 3.18 (dd, J=6.8, 4.8 Hz, 1 H), 2.98 (ddq, J=10.1, 6.9, 6.9 Hz, 1 H), 2.78 (ddq, J=9.8, 6.8, 6.8 Hz, 1 H), 2.66 (qd, J=7.3, 4.6 z, 1 H), 2.60-2.55 (m, 1 H), 2.10-1.80 (m, 10 H), 1.69 (ddd,

J=14.4, 10.3, 3.1 Hz, 1 H), 1.64 (d, J=1.3 Hz, 3 H), 1.30 (d, J=7.4 Hz, 3 H), 1.06 (d, J=6.9 Hz, 3 H), 1.00 (d, J=6.8 Hz, 3 H), 0.99 (d, J=6.7 Hz, 3 H), 0.97 (d, J=6.8 Hz, 3 H), 0.94 (d, J=6.8 Hz, 3 H), 0.82 (d, J=6.3 Hz, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 173.6, 157.0, 134.4, 133.7, 133.4, 132.9, 132.2, 129.9, 129.8, 117.9, 79.1, 78.9, 77.9, 75.7, 73.2, 64.4, 43.1, 41.0, 37.4, 36.1, 36.0, 35.8, 35.3, 34.8, 33.1, 23.3, 18.4, 17.4, 15.6, 15.5, 13.7, 12.5, 9.0; high resolution mass spectrum (FAB, NBA) m/z 616.3840 [(M+Na)⁺ ; calcd for C₃₃ H₅₅ NO₈ Na: 616.3826].

EXAMPLE 51 (FIGS. 16 and 17)

A. Tosylate 101

A solution of diene 16 (see, Smith, et al., J. Am. Chem. Soc. 1995, 117, 12011) (1.15 g, 1.0 mmol) in anhydrous pyridine (10 mL) at 0° C. is treated with p-toluenesulfonyl chloride (286 mg, 1.5 mmol). The mixture is allowed to warm to room temperature for 4-6 h. The pyridine is removed in vacuo and the residue is purified by flash chromatography to afford tosylate 101.

B. Arene 102

Phenyllithium (2.7 mL, 1.8 M in cyclohexane-ether (70:30)) is added dropwise to a solution of copper (I) iodide (460 mg, 2.4 mmol) in anhydrous diethyl ether (5 mL) at 0° C. To the resultant mixture is added a solution of tosylate 101 (780 mg, 0.6 mmol) in ether (5 mL) and the resultant mixture is warmed to room temperature with stirring. After 4 h, saturated aqueous ammonium chloride (20 mL) is added. The layers are separated and the aqueous layer is extracted with ethyl acetate. The combined organics are dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 102.

C. Lactol 103

To a solution of 102 (120 mg, 0.1 mmol) in tetrahydrofuran-acetonitrile (15 mL, 2:1) is added phosphate buffer (pH 7, 5 mL) and mercury (II) chloride (272 mg, 1.0 mmol). The resultant mixture is stirred 1 h at room temperature. The reaction mixture is diluted with ether (100 mL) and washed with saturated aqueous brine (2×50 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 103 as a mixture of α and β anomers.

D. Lactone 104

To a solution of 103 (84 mg, 0.070 mmol) in dimethyl sulfoxide (10 mL) is added acetic anhydride (2 mL). After 2 days at room temperature, the mixture is diluted with ether (100 mL) and washed with saturated aqueous sodium bicarbonate (50 mL), saturated aqueous brine (50 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 104.

E. Alcohol 105

To a solution of 104 (56 mg, 0.050 mmol) in dichloromethane (3 mL) at 0° C. is added water (50 mL) and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (52 mg, 0.018 mmol). After 1 h, the reaction mixture is diluted with ethyl acetate (50 mL), washed with saturated aqueous brine (3×25 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 105.

F. Carbamate 106

To a solution of 105 (10 mg, 0.010 mmol) in dichloromethane (2 mL) is added trichloroacetyl isocyanate (0.12 mL, 1.00 mmol). After 30 min, the reaction mixture is diluted with dichloromethane (4 mL) and neutral alumina (1 g) is added. The resultant suspension is stirred an additional 4 h. The reaction mixture is filtered and the concentrated filtrate is chromatographed on silica gel to afford 106.

G. Tetrol 107

A solution of 106 (10 mg, 0.0096 mmol) in 48% hydrofluoric acid-acetonitrile (1:9, 2 mL) is stirred at ambient temperature. After 12 h, saturated aqueous sodium bicarbonate (25 mL) is added and the mixture is extracted with ethyl acetate (3×20 mL). The combined organics are dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 107.

EXAMPLE 52 (FIGS. 18-20)

A. Alcohol 203

To a slurry of powdered 4-Å molecular sieves (2.0 g) in 100 mL of anhydrous toluene is added boronate 202 (see, Roush, et al., J. Am. Chem. Soc. 1990, 112, 6348) (170 mL, 1.0 M in toluene). The resultant solution is stirred 10 min at room temperature and then cooled to -78° C. A solution of aldehyde 201 (see, Solladie, et al., Tetrahedron Lett. 1987, 28, 797) (113 mmol) in toluene (100 mL) is added over a 2 h period, after which the reaction is maintained at -78° C. for 10 h. Excess ethanolic sodium borohydride (ca. 0.75 g/10 mL) is added and the reaction mixture is warmed to 0° C. Aqueous 1 N sodium hydroxide (300 mL) is added and the mixture is stirred vigorously for 2 h. The layers are separated and the aqueous layer is extracted with ether (5×300 mL). The combined organics are dried over potassium carbonate and concentrated in vacuo. The residue is purified by flash chromatography to afford 203.

B. Bis-silyl ether 204

A solution of 203 (75 mmol) in dimethylformamide (150 mL) is cooled to 0° C. and treated with imidazole (150 mmol) and tert-butyldimethylsilyl chloride (100 mmol). The resultant solution is warmed to room temperature. After 12 h, the reaction mixture is poured into 1500 mL of water and.extracted with ether (3×200 mL). The ethereal extracts are washed with water (2×50 mL) and saturated aqueous brine (50 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 204.

C. Alcohol 205

A solution of 204 (20 mmol) in 500 mL of methanol is cooled to -78° C. and treated with a stream of ozone and oxygen until the colorless solution is converted into a steel blue one. The crude reaction mixture is cautiously quenched with sodium borohydride (100 mmol) and the resultant solution is warmed to room temperature. After 3 h, the excess sodium borohydride is destroyed by the cautious addition of water. The methanol is removed in vacuo and the residue is partitioned between saturated aqueous ammonium chloride (200 mL) and ethyl acetate (200 mL). The layers are separated and the aqueous layer is further extracted with ethyl acetate (2×100 mL). The combined organics are dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 205.

D. Triethylsilyl ether 206

A solution of 205 (15 mmol) in dimethylformamide (30 mL) is cooled to 0° C. and treated with imidazole (30 mmol) and triethylsilyl chloride (20 mmol). The resultant solution is warmed to room temperature. After 12 h, the reaction mixture is poured into 300 mL of water and extracted with ether (3×40 mL). The ethereal extracts are washed with water (2×25 mL) and saturated aqueous brine (25 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 206.

E. Alcohol 207

To a solution of 206 (6 mmol) in ethyl acetate-ethanol (8:1, 90 mL) is added palladium on carbon (10% wet, 500 mg). The mixture is stirred under hydrogen atmosphere for 3-6 h, then filtered and concentrated in vacuo. The residue is purified by flash chromatography to afford 207.

F. Aldehyde 208

To a -10° C. solution of 207 (13 mmol) and triethylamine (50 mmol) in dichloromethane (26 mL) is added a solution of sulfur trioxide-pyridine (39 mmol) in dimethyl sulfoxide (50 mL). The mixture is stirred 1 h at room temperature and diluted with ether (150 mL). The organic phase is washed with aqueous sodium bisulfate (1 M, 100 mL), saturated aqueous brine (4×100 mL), dried over magnesium sulfate, and concentrated in vacuo. The residue is purified by flash chromatography to afford 208.

G. Wittig product 209

Phosphonium salt 15 (see, Smith, et al., J. Am. Chem. Soc. 1995, 117, 12011) (0.2 mmol) is dissolved in anhydrous tetrahydrofuran (2 mL) and chilled to 0° C. A solution of sodium bis(trimethylsilyl)amide (0.2 mmol, 1.0 M in tetrahydrofuran) is added and the reaction mixture is stirred 30 min at 0° C. After cooling to -78° C., a solution of aldehyde 208 (0.1 mmol) in tetrahydrofuran (2 mL) is added and the mixture is stirred 10 min at -78° C. and 2 h at room temperature. Saturated aqueous ammonium chloride (2 mL) is added and the resultant mixture is extracted with ether (3×20 mL). The ethereal layer is washed with water (2×25 mL) and saturated aqueous brine (25 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 209.

H. Hydroxy diene 210

A -78° C. solution of 209 (0.05 mmol) in CH₂ Cl₂ (5 mL) is treated with diisobutylaluminum hydride (0.5 mL, 1.0 M in toluene). The resultant solution is stirred 10 min at -78° C. and 30 min at 0° C. The reaction is quenched with a saturated solution of sodium potassium tartrate (50 mL) and the mixture is diluted with ether (60 mL). The organic layer is separated, dried over magnesium sulfate, and concentrated in vacuo. The residue is purified by flash chromatography to afford 210.

I. Aldehyde 211.

To a -10° C. solution of 207 (1.3 mmol) and triethylamine (5.0 mmol) in dichloromethane (3 mL) is added a solution of sulfur trioxide-pyridine (3.9 mmol) in dimethyl sulfoxide (5 mL). The mixture is stirred 1 h at room temperature and diluted with ether (15 mL). The organic phase is washed with aqueous sodium bisulfate (1 M, 10 mL), saturated aqueous brine (4×10 mL), dried over magnesium sulfate, and concentrated in vacuo. The residue is purified by flash chromatography to afford 211.

J. Tetraene 212

A solution of diphenylallylphosphine (0.08 mL, 0.38 mmol) in tetrahydrofuran (2 mL) is cooled to -78° C. and tert-butyllithium (0.14 mL, 1.7 M in pentane) is added. The mixture is warmed to 0° C. for 30 min, then recooled to -78° C. and treated with titanium (IV) isopropoxide (0.30 mmol). After 30 min, aldehyde 211 (0.30 mmol) is introduced as a solution in tetrahydrofuran (2 mL). The resultant solution is stirred at -78° C. for 15 min and at 0° C. for 1 h. Methyl iodide (0.64 mmol) is added, and the reaction is warmed to room temperature for 12 h. The reaction mixture is diluted with ether (60 mL), washed with aqueous sodium bisulfate (30 mL, 1.0 M), saturated aqueous brine (30 mL), and is dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 212.

K. Aldehyde 213

Oxalyl chloride (1.5 mmol) is added dropwise to a -78° C. solution of dimethyl sulfoxide (3 mmol) in dichloromethane (4 mL). After 15 min, a -78° C. solution of 212 (1 mmol) in dichloromethane (2 mL) is added via canula. After an additional 15 min, diisopropylethylamine (4.5 mmol) is added and the reaction is gradually warmed to room temperature over 1 h and quenched with aqueous sodium bisulfate. The mixture is diluted with ether (50 mL) and is washed with water (2×30 mL), saturated aqueous brine (2×30 mL), is dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 213.

L. Ester 214

To a -78° C. solution of (F₃ CCH₂ O)₂ POCH₂ CO₂ Et (2 mmol) and 18-crown-6 (2.4 mmol) in tetrahydrofuran (5 mL) is added potassium bis (trimethylsilyl) amide (2 mmol) in tetrahydrofuran (2 mL). The resultant solution is stirred 10 min at -78° C. and then treated with aldehyde 213 (1.2 mmol) in 4 mL of tetrahydrofuran. The reaction mixture is warmed to 0° C. for 6-8 h and then quenched with saturated aqueous ammonium chloride (10 mL). The aqueous layer is separated and extracted with hexane (2×25 mL). The combined organics are dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 214.

M. Alcohol 215

To a solution of 214 (0.050 mmol) in dichloromethane (3 mL) at 0° C. is added water (50 mL) and 2, 3-dichloro-5, 6-dicyano-1,4-benzoquinone (0.018 mmol). After 1 h, the reaction mixture is diluted with ethyl acetate (50 mL), washed with saturated aqueous brine (3×25 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 215.

N. Carbamate 216

To a solution of 215 (0.010 mmol) in dichloromethane (2 mL) is added trichloroacetyl isocyanate (1.00 mmol). After 30 min, the reaction mixture is diluted with dichloromethane (4 mL) and neutral alumina (1 g) is added. The resultant suspension is stirred an additional 4 h. The reaction mixture is filtered and the concentrated filtrate is chromatographed on silica gel to afford 216.

O. Triol 217

A solution of 216 (0.010 mmol) in 48% hydrofluoric acid-acetonitrile (1:9, 2 mL) is stirred at ambient temperature. After 12 h, saturated aqueous sodium bicarbonate (25 mL) is added and the mixture is extracted with ethyl acetate (3×20 mL). The combined organics are dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 217.

EXAMPLE 53 (FIGS. 21 and 22)

A. Hydroxy-oxazole 302

A solution of oxazole (3 mmol) in tetrahydrofuran (15 mL) is cooled to -78° C. and treated with n-BuLi (3 mmol) in hexane. (see, Hodges, et al., J. Org. Chem. 1991, 56, 449). After 30 min at -78° C., previously prepared (see, Smith, et al., J. Am. Chem. Soc. 1995, 117, 12011) aldehyde 301 (2 mmol) is added in tetrahydrofuran (10 mL) and the reaction mixture is gradually allowed to warm to room temperature. After 18-24 h, the reaction is quenched by addition of saturated aqueous ammonium chloride (25 mL). The aqueous layer is separated and extracted with ether (3×25 mL). The combined organics are dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 302.

B. Tosylate 303

A solution of 302 (1.0 mmol) in anhydrous pyridine (10 mL) at 0° C. is treated with p-toluenesulfonyl chloride (286 mg, 1.5 mmol) The mixture is allowed to warm to room temperature for 4-6 h. The pyridine is removed in vacuo and the residue is purified by flash chromatography to afford tosylate 303.

C. Reduction product 304

To a 0° C. solution of tosylate 303 (0.5 mmol) in tetrahydrofuran (2 mL) is added lithium triethylborohydride (2 mmol) as a solution in tetrahydrofuran (1.0 M). The resultant solution is warmed to room temperature for 2-4 h and then quenched with water (1 mL) and diluted with ether (25 mL). The ethereal layer is washed with saturated aqueous brine (2×10 mL), dried over magnesium sulfate, and concentrated in vacuo.

The residue is purified by flash chromatography to afford 304.

D. Lactol 305

To a solution of 304 (0.1 mmol) in tetrahydrofuran-acetonitrile (15 mL, 2:1) is added phosphate buffer (pH 7, 5 mL) and mercury (II) chloride (1.0 mol). The resultant mixture is stirred 1 h at room temperature. The reaction mixture is diluted with ether (100 mL) and washed with saturated aqueous brine (2×50 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 305 as a mixture of α and β anomers.

E. Lactone 306

To a solution of 305 (0.070 mmol) in dimethyl sulfoxide (10 mL) is added acetic anhydride (2 mL). After 2 days at room temperature, the mixture is diluted with ether (100 mL) and washed with saturated aqueous sodium bicarbonate (50 mL), saturated aqueous brine (50 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 306.

F. Alcohol 307

To a solution of 306 (0.050 mmol) in dichloromethane (3 mL) at 0° C. is added water (50 mL) and 2,3-dichloro-5, 6-dicyano-1,4-benzoquinone (0.018 mmol). After 1 h, the reaction mixture is diluted with ethyl acetate (50 mL), washed with saturated aqueous brine (3×25 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 307.

G. Carbamate 308

To a solution of 307 (0.010 mmol) in dichloromethane (2 mL) is added trichloroacetyl isocyanate (1.00 mmol). After 30 min, the reaction mixture is diluted with dichloromethane (4 mL) and neutral alumina (1 g) is added. The resultant suspension is stirred an additional 4 h. The reaction mixture is filtered and the concentrated filtrate is chromatographed on silica gel to afford 308.

H. Tetrol 309

A solution of 308 (0.010 mmol) in 48% hydrofluoric acid-acetonitrile (1:9, 2 mL) is stirred at ambient temperature. After 12 h, saturated aqueous sodium bicarbonate (25 mL) is added and the mixture is extracted with ethyl acetate (3×20 mL). The combined organics are dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 309.

EXAMPLE 54

As shown in FIG. 23, a solution of 402 (10.5 mg, 10.4 mmol) in 48% HF-CH₃ CN (1:9, 1.0 mL) is stirred at room temperature for 12 hr. The reaction is quenched by saturated NaHCO₃ (5.0 mL). The mixture is extracted with ethyl acetate (3×10 mL). The combined organic phase is then washed with brine (5.0 mL), dried over MgSO₄₁ concentrated in vacuo. The residue is purified by flash chromatography to afford 401.

EXAMPLE 55 (FIG. 24)

A. PMB-ether 503

ZnCl₂ (1.32 g, 9.69 mmol) is dried at 160° C. under vacuum overnight and then treated with a solution of iodide 502 (2.46 g, 9.59 mmol) in dry Et₂ O (50 mL). The mixture is stirred at room temperature until most of the ZnCl₂ is dissolved and then cooled to -78° C. t-BuLi (1.7M in pentane, 17.0 mL) is added over 30 min, and the resultant solution is stirred an additional 15 min, warmed to room temperature, and stirred for 1 hr. The solution is added by cannula to a mixture of iodoolefin B (see, Smith, et al., J. Am. Chem. Soc. 1995, 117, 12011) (3.21 g, 6.19 mmol) and Pd(PPh₃)₄ (364.2 mg, 0.315 mmol). The mixture is covered with aluminum foil, stirred overnight, and then diluted with ethyl acetate(100 mL), washed with brine (2×100 mL), dried over MgSO₄, filtered and concentrated in vacuo. The residue is purified by flash chromatography to afford 503.

B. Phosphonium salt 504

A solution of alcohol 503 (1.70 g, 3.26 mmol) in CH₂ Cl₂ (28 mL) is cooled to 0° C. and treated with water (1.3 mL) and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (774 mg, 3.41 mmol). The mixture is stirred at 0° C. for 5 hr, diluted with CH₂ Cl₂ (20 mL), dried over MgSO₄, and filtered through a column of silica gel. Following concentration in vacuo, the residue is dissolved in ethanol (50 mL) at room temperature, and excess sodium borohydride is added. After 30 min, the reaction is cooled to 0° C., quenched with saturated aqueous NH₄ Cl (50 mL), and concentrated. The residue is then dissolved in CH₂ Cl₂ (90 mL), and the solution is washed with water, dried over MgSO₄₁ filtered and concentrated in vacuo. The residue is purified by flash chromatography to afford an alcohol

A solution of this alcohol (400 mg, 1.0 mmol) in dry benzene/ether (1:2, 50 mL) is treated with triphenylphosphine (923 mg, 3.6 mmol) and imidazole (273 mg, 4.0 mmol). After all of the imidazole dissolved, iodine (761 mg, 3.0 mmol) is added with vigorous stirring of the reaction mixture. The mixture is stirred 2 h further and then treated with triethylamine (4 mL). The resultant solution is diluted with CH₂ Cl₂ (50 mL) and washed with saturated aqueous Na₂ S₂ O₃ (100 mL), saturated aqueous NaHCO₃ (100 mL), and brine (2×100 mL). The organic phase is dried over MgSO₄, filtered and concentrated in vacuo. Filtration though silica gel to remove triphenylphosphine oxide, affords an iodide. The iodide was mixed with diisopropylethylamine (0.6 mL, 3.44 mmol) and triphenylphosphine (4.94 g, 18.8 mmol). The mixture is heated at 80° C. for 24 hr, cooled to room temperature, and washed with hexane(2×50 mL). The product is isolated by flash chromatography to afford 504.

C. Coupled product 505

Phosphonium salt 504 (386 mg, 0.5 mmol) is dried azeotropically with dry benzene and heated at 50° C. under vacuum for 3 hr before use. It is then dissolved in tetrahydrofuran (3.0 mL). Sodium bis(trimethylsilyl)amide (1.0 M in tetrahydrofuran, 0.48 mL, 0.48 mmol) is added at -78° C., and the mixture is stirred for 25 min and then recooled to -78° C. A solution of aldehyde C (see, Smith, et al., J. Am. Chem. Soc. 1995, 117, 12011) (147 mg, 0.30 mmol) in tetrahydrofuran (1.5 mL) is added, and the mixture is stirred for 10 min at -78° C., and 2 hr at room temperature. The reaction is quenched with saturated aqueous NH₄ Cl (4.0 mL), the resultant mixture is extracted with ether (120 mL), and the ether layer is washed with water (100 mL) and brine(100 mL), dried over MgSO₄, filtered and concentrated in vacuo. Flash chromatography provides olefin 505.

D. Lactone 506

To a solution of 505 (200 mg, 0.23 mmol) in tetrahydrofuran-acetonitrile (10 mL, 2:1) is added a phosphate buffer solution (pH=7.0, 3.3 mL), and HgCl₂ (1.3 g). The suspension is stirred at room temperature for 40 min, then diluted with ether (150 mL), washed with brine (2×70 mL), dried over MgSO₄, and concentrated in vacuo. Flash 20 chromatography provides a mixture of lactols as α/β anomers. This material is used directly in the next oxidation: Under argon, to a solution of lactols in dimethylsulfoxide (5.0 mL) is added acetic anhydride (1.0 mL). After 2 days at room temperature, the mixture is diluted with ether (150 mL), washed with saturated NaHCO₃ (150 mL), brine(150 mL), dried over MgSO₄, and concentrated in vacuo. Flash chromatography affords a lactone. A solution of the lactone (160 mg, 0.20 mmol) in methanol (4 mL) is treated with pyridinium p-toluenesulfonate (10 mg) and stirred at 40° C. for 30 min. The mixture is diluted with ether (80 mL) and washed successively with saturated aqueous NaHCO₃ solution (90 mL) and brine (40 mL), and then dried over MgSO₄. The organic solution is concentrated in vacuo, and the residue is passed through a column of silica gel to provide alcohol 506.

E. Acid 507

To a solution of alcohol 506 (140 mg, 0.19 mmol) in dimethylformamide (5.0 mL), is added pyridinium dichromate (210 mg, 0.55 mmol). The reaction mixture is stirred at room temperature for 5 hr, and diluted with water (120 mL). The mixture is extracted with ether (3×15 mL). The organic solutions are combined and washed with brine (40 mL), and dried over MgSO₄. Then it is concentrated in vacuo to give a residue, which is purified by flash chromatography to afford carboxylic acid 507.

F. Amino-amide 508

To a solution of 507 (60.0 mg, 78.1 mmol) and D-leucine hydrochloride (26.0 mg, 0.16 mmol) in CH₂ Cl₂ (3 mL) is added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 23 mg, 0.12 mmol) and 1-hydroxybenzotriazole (21.0 mg, 0.14 mmol), followed by diisopropylamine (40 mL, 0.23 mmol). The mixture is stirred at room temperature overnight before addition of 5% KHSO₄ solution. The resulting mixture is extracted with ethyl acetate (30 mL). The organic layer is washed with brine (20 mL) and dried over MgSO₄, and then concentrated in vacuo. The residue is purified by column chromatography to afford 508.

G. Analog 501

A solution of 508 (52 mg, 59 mmol) in 48% HF-acetonitrile(1:9, 1.0 mL) is stirred at room temperature for 12 hr. The reaction is quenched by saturated NaHCO₃ (5.OmL). The mixture is extracted with ethyl acetate (3×10 mL). The combined organic phase is then washed with brine (5.0 mL), dried over MgSO₄, and concentrated in vacuo. Flash chromatography provides 501.

EXAMPLE 56 (FIG. 25)

A. Diene 603

Phosphonium salt 15 (98.0 mg, 0.092 mmol) is dried azeotropically with dry benzene and heated at 50° C. under vacuum for 3 hr before use. It is then dissolved in tetrahydrofuran (0.7 mL). Sodium bis(trimethylsilyl)amide (1.0 M in tetrahydrofuran, 86 mL, 0.0855 mmol) is added at -78° C., and the mixture is stirred for 20 min and then recooled to -78° C. A solution of aldehyde 602 (13 mg, 60 mmol) in tetrahydrofuran (300 mL) is added, and the mixture is stirred for 10 min at -78° C., and 2 hr at room temperature. The reaction is quenched with saturated aqueous NH₄ Cl (1.0 mL). The resultant mixture is extracted with ether (30 mL), and the ether layer is washed with water (30 mL) and brine (30 mL), dried over MgSO₄, filtered and concentrated in vacuo. Flash chromatography provides the coupled product.

A solution of the olefin (39 mg, 44 mmol) in CH₂ Cl₂ is cooled to -78° C., diisobutylaluminum hydride (1.0 M in toluene, 440 mL, 0.40 mmol) is added dropwise over 5 min, and the resultant solution is stirred for 10 min at -78° C. and 30 min at 0° C. The reaction is quenched with a saturated solution of Rochelle's salt, and the mixture is diluted with ether (60 mL), washed with Rochelle solution, and brine(30 mL each), dried over MgSO₄, filtered and concentrated in vacuo. Flash chromatography provides alcohol 603.

B. Alkane 604

To a solution of alcohol 603 (82 mg, 0.93 mmol) in pyridine (1.5 mL) at 0° C. is added p-toluenesulfonyl chloride(26.6 mg, 0.14 mmol) with stirring. After 3 hr, the reaction mixture is concentrated in vacuo. The residue is purified by column chromatography to give a tosylate. To a solution of this tosylate (94 mg, 0.91 mmol) in ether (5 mL) is added lithium diisopropylcuprate (Pr₂ CuLi) (ca. 0.5 M in ether, 10 mL, excess. The resultant solution is stirred for 8 hr and then quenched with saturated aqueous solution of NH₄ Cl (50 mL). Stirring is continued for an additional 2 h. The organic phase is separated and washed with NH₄ Cl solution (20 mL), dried over MgSO₄, and concentrated in vacuo. Flash chromatography provides 604.

C. Enone 605

A solution of 604 (75 mg, 83 mmol) in methanol (2 mL) is treated with pyridinium p-toluenesulfonate (ca.4 mg) and stirred at 40° C. for 30 min. The mixture is diluted with ether (20 mL) and washed successively with saturated aqueous NaHCO3 solution (25 mL) and brine (10 mL), and then dried over MgSO₄. The organic solution is concentrated in vacuo, and the residue is passed through a column of silica gel to provide an alcohol. To a solution of the alcohol (62.0 mg, 68.2 mmol) in benzene (2.0 mL) is added manganese(IV) oxide (100 mg, 1.15 mmol). After stirring for 8 h at room temperature, the reaction mixture is filtered through a pad of celite. The filtrate is concentrated in vacuo. Flash chromatography of the residue affords α,βp-unsaturated ketone 605.

D. Triol 606

A solution of the α,β-unsaturated ketone 605 (45 mg, 56 mmol) in CH₂ Cl₂ (2 mL) is cooled to 0° C. and treated with water (0.1 mL) and 2, 3-dichloro-5, 6-dicyano-1, 4-benzoquinone (15 mg, 66 mmol). The mixture is stirred at 0° C. for 5 hr, diluted with CH₂ Cl₂ (15 mL), dried over MgSO₄, and filtered through a column of silica gel. Following concentration in vacuo, the residue is used for next step without further purification. A solution of the crude alcohol in 48% HF-acetonitrile(1:9, 1.0 mL) is stirred at room temperature for 12 hr. The reaction is quenched by saturated NaHCO₃ (5.OmL). The mixture is extracted with ethyl acetate(3×10 mL). The combined organic phase is then washed with brine (5.0 mL), dried over MgSO₄, concentrated in vacuo. The residue is purified by flash chromatography to afford 601.

EXAMPLE 57 (FIG. 26)

A. Alkane 702

To a solution of iodide A (300 mg, 0.54 mmol) in ether (5 mL) is added lithium dibutylcuprate (Bu₂ CuLi) (ca. 0.5 M in ether, 5.4 mL, excess) at -25° C. The resultant solution is stirred for 8 hr and then quenched with saturated aqueous NH₄ Cl (50 mL). Stirring is continued for another 2 hr and the organic phase is separated. The organic solution is washed with NH₄ Cl solution (20 mL) and dried over MgSO₄, and concentrated in vacuo. Flash chromatography provides 702.

B. Alcohol 703

A solution of 702 (240 mg, 0.50 mmol) in CH₂ Cl₂ (6.0 mL) is cooled to -78° C. Diisobutylaluminum hydride (1.0 M in toluene, 1.50 mL, 1.50 mmol) is added dropwise over 5 min, and the resultant solution is stirred for 10 min at -78° C. and 30 min at 0° C. The reaction is quenched with a saturated solution of Rochelle's salt, and the mixture is diluted with ether (60 mL), washed with Rochelle solution, and brine (30 mL each), dried over MgSO₄, filtered and concentrated in vacuo. Flash chromatography provides alcohol 703.

C. Iodide 704

A solution of alcohol 703 (210 mg, 0.44 mmol) in dry benzene/ether (1:2, 5 mL) is treated with triphenylphosphine (420 mg, 1.6 mmol) and imidazole (123 mg, 1.8 mmol). After all of the imidazole dissolved, iodine (335 mg, 1.32 mmol) is added with vigorous stirring. The mixture is stirred for 2 h and then treated with triethylamine (1.8 mL). The resultant solution is diluted with CH₂ Cl₂ (22 mL) and washed with saturated aqueous Na₂ S₂ O₃ (40 mL), saturated aqueous NaHCO₃ (40 mL), and brine (2×40 mL). The organic phase is dried over MgSO₄, filtered and concentrated in vacuo. The residue is purified by flash chromatography to afford iodide 704.

D. Phosphonium salt 705

The iodide 704 is mixed with triphenylphosphine (2.17 g, 8.27 mmol) and the mixture is heated at 80° C. for 24 hr, cooled to room temperature, and washed with hexane (2×20 mL) Flash chromatography provides phosphonium salt 705.

E. Alkene 707

A solution of 705 (260 mg, 0.30 mmol) in tetrahydrofuran (6.0 mL) is cooled to -10° C. and a solution of n-butyl lithium (1.0 M in hexane, 0.29 mL, 0.29 mmol) is introduced dropwise over 5 min. The resultant solution is stirred for 50 min at room temperature and then the mixture is recooled to -78° C. and aldehyde 706 (39 mg, 0.3 mmol) is added a solution in tetrahydrofuran (1.5 mL). The mixture is stirred for 10 min at -78° C., and 1 hr at 0° C. The reaction is quenched with saturated aqueous NH₄ Cl (1.0 mL) and the resultant mixture is extracted with ether (30 mL). The ether layer is washed with water (30 mL) and brine (30 mL), dried over MgSO₄, filtered and concentrated in vacuo. The residue is purified by flash chromatography to afford olefin 707 (149 mg, 85% yield).

F. Diol 708

Acetonide 707 (147 mg, 0.25 mmol) is dissolved in 80% aqueous acetic acid (2.5 mL) at room temperature. The reaction mixture is stirred for 4 hr at room temperature and then diluted with water (20 mL). The mixture is extracted with ethyl acetate (2×5 mL). The combined organic layers are washed with saturated NaHCO₃ solution, and brine (10 mL each), and then dried over MgSO₄. The organic solution is concentrated in vacuo, and the residue is flash chromatographed over silica gel to afford diol 708.

G. Tosylate 709

To a solution of diol 708 (134 mg, 0.25 mmol) in pyridine (2 mL) is added p-toluenesulfonyl chloride(52 mg, 0.27 mmol). After 3 hr, the reaction mixture is diluted with ether (30 mL), and washed with ice cold 1 M hydrochloric acid (60 mL), saturated NaHCO₃ solution (20 mL), and brine (20 mL) and then concentrated in vacuo. The residue is purified by column chromatography to give a monotosylate 709.

H. Epoxide 710.

A solution of tosylate 709 (145 mg, 0.21 mmol) in methanol (3.0 mL) is added potassium carbonate (10 mg) at room temperature. The mixture is stirred for 20 min, and then diluted with water (60 mL) and extracted with ethyl acetate (2×20 mL). The combined organic layers are washed with brine and concentrated in vacuo. Flash chromatography provides epoxide 710.

I. Alcohol 711.

To a solution of 710 (41 mg, 79 mmol) in CH₂ Cl₂ (3.0 mL) at 0° C. is added water (0.15 mL) and 2,3-dichloro-5,6-dicyano-1, 4-benzoquinone (60 mg, 0.26 mmol). The mixture is stirred at 0° C. for 5 hr, diluted with CH₂ Cl₂ (15 mL), dried over MgSO₄, and filtered through a column of silica gel. Following concentration in vacuo, the crude 711 is used without further purification.

J. Carbamate 712

To a solution of 711 (8.7 mg, 22 mmol) in CH₂ Cl₂ (1.0 mL) is added trichloroacetyl isocyanate (0.20 mL, 1.7 mmol) at room temperature. After 30 min, the mixture is diluted with CH₂ Cl₂ (20 mL), and some neutral Al₂ O₃ (500 mg) is added. The mixture is then stirred at room temperature for 2 hr, then filtered though a short column of silica gel, and concentrated in vacuo. The residue is purified by flash chromatography to afford 712.

K. Hydroxy-urethane 701

A solution of 712 (6.0 mg, 14 mmol) in 48% HF-acetonitrile (1:9, 1.0 mL) is stirred at room temperature for 12 hr. The reaction is quenched by saturated NaHCO₃ (5.0 mL). The mixture is extracted with ethyl acetate (3×10 mL). The combined organic phase is then washed with brine (5.0 mL), dried over MgSO₄, and concentrated in vacuo. The residue is purified by flash chromatography afford 701.

EXAMPLE 58 (FIGS. 27 and 28)

A. Iodide 802

A solution of alcohol 16 (see, Smith, et al., J. Am.

Chem. Soc. 1995, 117, 12011) (410 mg, 0.360 mmol) in dry benzene/ether (1:2, 10 mL) is treated with triphenylphosphine (378 mg, 1.44 mmol) and imidazole (111 mg, 1.62 mmol). After complete dissolution of the imidazole, iodine (301 mg, 1.19 mmol) is added with vigorous stirring. The reaction mixture is stirred 2 h and then treated with triethylamine (1.7 mL). The resultant solution is diluted with CH₂ Cl₂ (30 mL) and washed with saturated aqueous Na₂ S₂ O₃ (40 mL), saturated aqueous NaHCO₃ (40 mL), and brine (2×40 mL). The organic phase is dried over MgSO₄, filtered and concentrated in vacuo. Purification of the residue by flash chromatography affords iodide 802.

B. Phosphonium salt 803

To a solution of iodide 802 (410 mg, 0.325 mmol) in benzene (20 mL) is added triphenylphosphine(1.00 g, 3.81 mmol) The mixture is heated at 80° C. for 24 hr, cooled to room temperature, and concentrated in vacuo. The residue is washed with hexane (2×20 mL). Flash chromatography affords phosphonium salt 803.

C. Alkene 805

A solution of 803 (460 mg, 0.30 mmol) in tetrahydrofuran (9.0 mL) is cooled to -10° C. A solution of n-butyl lithium (1.0 M in hexane, 0.29 mL, 0.29 mmol) is added dropwise over 5 min, and the resultant solution is stirred for 50 min at room temperature. Then the mixture is recooled to -78° C. and a solution of aldehyde 804 (39 mg, 0.3 mmol) in tetrahydrofuran (1.5 mL) is added. The mixture is stirred for 10 min at -78° C., and 1 hr at 0° C. The reaction is quenched with saturated aqueous NH₄ Cl (20 mL), the resultant mixture is extracted with ether (40 mL), and the ether layer is washed with water (30 mL) and brine (30 mL), dried over MgSO₄, filtered and concentrated in vacuo. Flash chromatography of the residue affords 805.

D. Diol 806

Acetonide 805 (280 mg, 0.22 mmol) is dissolved in 80% aqueous acetic acid (3.5 mL) at room temperature. The reaction mixture is stirred for 4 hr at room temperature and then diluted with water (40 mL). The mixture is extracted with ethyl acetate (2×10 mL). The combined organic layers are washed with saturated NaHCO₃ solution, and brine (10 mL each), and then dried over MgSO₄. The organic solution is concentrated in vacuo, and the residue is flash chromatographed over silica gel to afford diol 806.

E. Tosylate 807

To a solution of diol 806 (235 mg, 0.19 mmol) in pyridine (2 mL) at 0° C. is added p-toluenesulfonyl chloride (45 mg, 0.23 mmol). After 3 hr, the reaction mixture is diluted with ether (30 mL), and washed with ice cold 1 M hydrochloric acid (30 mL), saturated NaHCO₃ solution (20 mL), and brine (20 mL) and then concentrated in vacuo. The residue is purified by column chromatography to give a monotosylate 807.

F. Epoxide 808

To a solution of tosylate 807 (187 mg, 0.21 mmol) in methanol (3.0 mL) is added potassium carbonate (10 mg) at room temperature. The mixture is stirred for 20 min, and then diluted with water (60 mL) and extracted with ethyl acetate (2×20 mL). The combined organic layers were washed with brine and concentrated in vacuo. Flash chromatography provides epoxide 808.

G. Lactone 809

To a solution of 808 (110 mg, 93 mmol) in tetrahydrofuran-acetonitrile (10 mL, 2:1) is added a phosphate buffer solution (pH=7.0, 3.5 mL), and HgCl₂ (2.3 g). The suspension is stirred at room temperature for 40 min, then diluted with ether (30 mL), washed with brine(2×30 mL), dried over MgSO₄, and concentrated in vacuo. Flash chromatography affords the lactol as an α/β anomeric mixture. This material is used directly in the next oxidation: Under argon atmosphere, a solution of the lactols in dimethylsulfoxide (3.0 mL) is treated with acetic anhydride (0.60 mL). After 2 days at room temperature, the mixture is diluted with ether (50 mL), washed with saturated NaHCO₃ (30 mL), brine (30 mL), dried over MgSO₄, and concentrated in vacuo. Flash chromatography provides 809.

H. Alcohol 810

To a solution of 809 (90 mg, 79 mmol) in CH₂ Cl₂ (3.0 mL) at 0° C. is added water (0.15 mL) and 2, 3-dichloro-5, 6-dicyano-1, 4-benzoquinone(60 mg, 0.26 mmol). The mixture is stirred at 0° C. for 5 hr, diluted with CH₂ Cl₂ (15 mL), dried over MgSO₄, and filtered through a column of silica gel. Following concentration in vacuo, the crude 810 is used in the next reaction without further purification.

I. Carbamate 811

To a solution of 810 (22 mg, 22 mmol) in CH₂ Cl₂ (1.0 mL) is added trichloroacetyl isocyanate (0.20 mL, 1.7 mmol) at room temperature. After 30 min, the mixture is diluted with CH₂ Cl₂ (20 mL), and some neutral Al₂ O₃ (500 mg) is added. The mixture is then stirred at room temperature for 2hr, then filtered though a short column of silica gel, and concentrated in vacuo. Flash chromatography affords 811.

J. Epoxide analog 812

A solution of 811 (15 mg, 14 mmol) in tetrahydrofuran(1.0 mL) is cooled to 0° C., and treated with a 1.0 M solution of tetrabutylammonium fluoride in tetrahydrofuran(0.14 mL, 0.14 mmol). The reaction mixture is stirred for 2 hr, and diluted with water (20 mL). The mixture is extracted with ethyl acetate (3×10 mL). The combined organic phase is then washed with brine (10 mL), dried over MgSO₄, concentrated in vacuo. Flash chromatography affords 801.

EXAMPLE 59 (FIG. 29)

A. Alcohol 903

Phosphonium salt 15 (98.0 mg, 0.092 mmol) is dried azeotropically with dry benzene and heated at 50° C. under vacuum for 3 hr before use. It is then dissolved in tetrahydrofuran (0.7 mL). Sodium bis(trimethylsilyl)amide (1.0 M in tetrahydrofuran, 86 mL, 0.0855 mmol) is added at -78° C., and the mixture is stirred for 20 min and then recooled to -78° C. A solution of aldehyde 902 (60 mmol) in tetrahydrofuran (300 mL) is added, and the mixture is stirred for 10 min at -78° C., and 2 hr at room temperature. The reaction is quenched with saturated aqueous NH₄ Cl (1.0 mL). The resultant mixture is extracted with ether (30 mL), and the ether layer is washed with water (30 mL) and brine (30 mL), dried over MgSO₄, filtered and concentrated in vacuo. Flash chromatography provides an olefin. A solution of the olefin (44 mmol) in CH₂ Cl₂ is cooled to -78° C. Diisobutylaluminum hydride (1.0 M in toluene, 440 mL, 0.40 mmol) is added dropwise over 5 min, and the resultant solution is stirred for 10 min at -78° C. and 30 min at 0° C. The reaction is quenched with a saturated solution of Rochelle's salt, and the mixture is diluted with ether (60 mL), washed with Rochelle solution, and brine (30 mL each), dried over MgSO₄₁ filtered and concentrated in vacuo. Flash chromatography provides alcohol 903.

B. Diene 905

A solution of 903 (0.012 mmol) and Et₃ N (42 mL, 0.30 mmol) in CH₂ Cl₂ (2.0 mL) is cooled to 0° C. and a solution of SO₃ -pyridine complex (40 mg, 0.251 mmol) in dimethylsulfoxide (0.6 mL) is added. The mixture is stirred at 0° C. for 45 min and then diluted with ethyl acetate (30 mL), washed with aqueous NaHSO₄ (1.0 M, 30 mL) and brine (2×30 mL), dried over MgSO₄, and concentrated in vacuo. Flash chromatography affords an aldehyde. A solution of allyldiphenylphosphine 904 (0.19 mmol) in tetrahydrofuran (1.0 mL) is cooled to -78° C. and t-butyl lithium (1.7 M in pentane, 0.122 mmol) is added. The mixture is stirred at 0° C. for 30 min, recooled to -78° C. and treated titanium tetra-I-propoxide (0.15 mmol). After 30 min, a cold (-78° C.) solution of the aldehyde (0.26 mmol) in tetrahydrofuran (1.0 mL) is introduced via cannula, and the mixture is stirred 10 min further at -78° C. and at 0° C. for 1 hr. Iodomethane (0.32 mmol) is added, and the reaction is maintained at 0° C. for 30 min, warmed to room temperature, protected from light, and stirred overnight. The reaction mixture is diluted with ether (30 mL), washed with 1.0 M aqueous NaHSO₄ and brine (30 mL each), dried over MgSO₄₁ concentrated in vacuo. Flash chromatography affords diene 905.

C. Glycoside 908

A solution of 905 (83 mmol) in methanol (2 mL) is treated with pyridinium p-toluenesulfonate (ca.4 mg) and stirred at 40° C. for 30 min. The mixture is diluted with ether (20 mL) and washed successively with saturated aqueous NaHCO₃ solution (25 mL) and brine (10 mL), and then dried over MgSO₄. The organic solution is concentrated in vacuo, and the residue is passed through a column of silica gel to give an alcohol.

To a solution of glycosyl bromide 906 (75 mmol) in CH₂ Cl₂ (2.0 mL) is added HgBr₂ (7 mmol) and powdered molecular sieves (4 Å, 50 mg) and stirred for 60 min at room temperature. The mixture is then cooled to 0° C., and the alcohol (74 mmol) prepared above is added in CH₂ Cl₂ (0.7 mL). The resultant mixture is stirred 6 hr at 0° C. and then warmed to room temperature and diluted with CH₂ Cl₂ (10 mL), and filtered through a pad of celite. The filtrate is washed with aqueous KI solution, and dried over MgSO₄. The organic solution is concentrated in vacuo, and the residue is passed through a column of silica gel to give an anomeric mixture of glycosides 908.

D. Triol 901

To a solution of 908 (79 mmol) in CH₂ Cl₂ (3.0 mL) at 0° C. is added water (0.15 mL) and 2, 3-dichloro-5, 6-dicyano-1, 4-benzoquinone (60 mg, 0.26 mmol). The mixture is stirred at 0° C. for 5 hr, diluted with CH₂ Cl₂ (15 mL), dried over MgSO₄, and filtered through a column of silica gel. Following concentration in vacuo, the crude alcohol is used for next step without further purification. To a solution of the alcohol (22 mmol) in CH₂ Cl₂ (1.0 mL) is added trichloroacetyl isocyanate (0.20 mL, 1.7 mmol) at room temperature. After 30 min, the mixture is diluted with CH₂ Cl₂ (20 mL), and some neutral Al₂ O₃ (500 mg) is added. The mixture is then stirred at room temperature for 2 hr, then filtered though a short column of silica gel, and concentrated in vacuo. Flash chromatography affords a carbamate. A solution of the carbamate (14 mmol) in 48% HF-acetonitrile (1:9, 1.0 mL) is stirred at room temperature for 12 hr. The reaction is quenched by saturated NaHCO₃ (5.0 mL). The mixture is extracted with ethyl acetate (3×10 mL). The combined organic phase is then washed with brine(5.0 mL), dried over MgSO₄, concentrated in vacuo. Flash chromatography affords 901.

EXAMPLE 60 (FIG. 30)

A. Olefin 1001

A solution of model phosphonium salt (0.0917 mmol) in THF (700 mL) is cooled to -78° C. and treated with NaHMDS (1.0 M in THF, 85.5 mL, 0.0855 mmol). The mixture is stirred for 20 min at 0° C., recooled to -78° C. and aldehyde C (0.0570 mmol) in THF (300 mL) is added. After 10 min at -78° C. and 2 h at room temperature, the mixture is quenched with saturated aqueous NH₄ Cl (1.0 mL) and extracted with ether (30 mL). The ether solution is washed with water, brine (30 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography provides olefin 1001.

B. Lactone 1002

A solution of olefin 1001 (0.00597 mmol) in THF/CH₃ CN (2:1, 1.50 mL) is treated with pH 7.0 phosphate buffer (500 mL) and HgCl₂ (215 mg). The suspension is stirred at room temperature for 40 min, diluted with ether (30 mL), washed with brine (2×30 mL), dried over MgSO₄, filtered and concentrated. Pipette flash chromatography (5% ethyl acetate/hexane) provides a mixture of lactols as a colorless oil which is further treated with DMSO (1.0 mL) and Ac₂ O (200 mL) at room temperature for 2 days. The mixture is diluted with ether (30 L), washed with saturated NaHCO₃ (30 mL), brine (30 mL), dried ver MgSO₄, filtered and concentrated. Flash chromatography rovides lactone 1002.

C. Model Compound 1003

A solution of olefin 1002 (5.5 mmol) in 48% HF--CH₃ CN (1:9, 1.0 mL) is stirred at room temperature for 12 h, then quenched with saturated aqueous NaHCO₃ (5.0 mL). The mixture is extracted with ethyl acetate (3×10 mL). The combined organic extracts are washed with brine (5.0 mL), dried over MgSO₄₁ filtered and concentrated. Pipette flash chromatography (gradient elution, 1:30 to 1:6 MeOH/CHCl13) provides 1003.

EXAMPLE 61 (FIGS. 31 and 32) I. General Procedure for Synthesis of Hydroxy Aldehydes 1104

A. TBS ether 1102a

A solution of bromide 1101a (see, Jacquesy, et al., Tetrahedron 1981, 37, 747) (20 mmol) in ether (40 mL) is added slowly to a -78° C. solution of tert-butyllitium (40 mmol, 1.7 M in pentane). After 1 h at -78° C., the cold solution is transferred to a suspension of copper (I) iodide (10 mmol) in ether at 0° C. After an additional 30 min at 0° C., a solution of benzyl (S)-(+)-glycidyl ether (9 mmol) in ether (20 mL) is added and the reaction is allowed to warm to room temperature. After 18-24 h, the reaction is quenched by the addition of tert-butyldimethylsilyl triflate (10 mmol). The reaction mixture is poured into saturated aqueous sodium bicarbonate (100 mL). The aqueous layer is separated and extracted with ether (2×50 mL). The combined organics are washed with saturated aqueous brine (50 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 1102a.

B. Alcohol 1103a

To a solution of 1102a (6 mmol) in ethyl acetate-ethanol (8:1, 90 mL) is added palladium on carbon (10% wet, 500 mg). The mixture is stirred under hydrogen atmosphere for 3-6 h, then filtered and concentrated in vacuo. The residue is purified by flash chromatography to afford 1103a.

C. Aldehyde 1104a.

Oxalyl chloride (1.5 mmol) is added dropwise to a -78° C. solution of dimethyl sulfoxide (3 mmol) in dichloromethane (4 mL). After 15 min, a -78° C. solution of 1103a (1 mmol) in dichloromethane (2 mL) is added via canula. After an additional 15 min, diisopropylethylamine (4.5 mmol) is added and the reaction is gradually warmed to room temperature over 1 h and quenched with aqueous sodium bisulfate. The mixture is diluted with ether (50 mL) and is washed with water (2×30 mL), saturated aqueous brine (2×30 mL), is dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 1104a.

II. General Procedure for the Conversion of 1104 to Arene Analog 1111

A. Diene 1105

Phosphonium salt 15 (see, Smith, et al., J. Am. Chem. Soc. 1995, 117, 12011) (0.2 mmol) is dissolved in anhydrous tetrahydrofuran (2 mL) and chilled to 0° C. A solution of sodium bis(trimethylsilyl)amide (0.2 mmol, 1.0 M in tetrahydrofuran) is added and the reaction mixture is stirred 30 min at 0° C. After cooling to -78° C., a solution of aldehyde 1104 (0.1 mmol) in tetrahydrofuran (2 mL) is added and the mixture is stirred 10 min at -78° C. and 2 h at room temperature. Saturated aqueous ammonium chloride (2 mL) is added and the resultant mixture is extracted with ether (3×20 mL). The ethereal layer is washed with water (2×25 mL) and saturated aqueous brine (25 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 1105.

B. Hydroxy diene 1106

A -78° C. solution of 1105 (0.05 mmol) in CH₂ Cl₂ (5 mL) is treated with diisobutylaluminum hydride (0.5 mL, 1.0 M in toluene). The resultant solution is stirred 10 min at -78° C. and 30 min at 0° C. The reaction is quenched with a saturated solution of sodium potassium tartrate (50 mL) and the mixture is diluted with ether (60 mL). The organic layer is separated, dried over magnesium sulfate, and concentrated in vacuo. The residue is purified by flash chromatography to afford 1106.

C. Aldehyde 1107

Oxalyl chloride (1.5 mmol) is added dropwise to a -78° C. solution of dimethyl sulfoxide (3 mmol) in dichloromethane (4 mL). After 15 min, a -78° C. solution of 1106 (1 mmol) in dichloromethane (2 mL) is added via canula. After an additional 15 min, diisopropylethylamine (4.5 mmol) is added and the reaction is gradually warmed to room temperature over 1 h and quenched with aqueous sodium bisulfate. The mixture is diluted with ether (50 mL) and is washed with water (2×30 mL), saturated aqueous brine (2×30 mL), is dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 1107.

D. Tetraene 1108

A solution of diphenylallylphosphine (0.08 mL, 0.38 mmol) in tetrahydrofuran (2 mL) is cooled to -78° C. and tert-butyllithium (0.14 mL, 1.7 M in pentane) is added. The mixture is warmed to 0° C. for 30 min, then recooled to -78° C. and treated with titanium (IV) isopropoxide (0.30 mmol). After 30 min, aldehyde 1107 (0.30 mmol) is introduced as a solution in tetrahydrofuran (2 mL). The resultant solution is stirred at -78° C. for 15 min and at 0° C. for 1 h. Methyl iodide (0.64 mmol) is added, and the reaction is warmed to room temperature for 12 h. The reaction mixture is diluted with ether (60 mL), washed with aqueous sodium bisulfate (30 mL, 1.0 M), saturated aqueous brine (30 mL), and is dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 1108.

E. Alcohol 1109

To a solution of 1108 (0.050 mmol) in dichloromethane (3 mL) at 0° C. is added water (50 mL) and 2,3-dichloro-5, 6-dicyano-1,4-benzoquinone (0.018 mmol). After 1 h, the reaction mixture is diluted with ethyl acetate (50 mL), washed with saturated aqueous brine (3×25 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 1109.

F. Carbamate 1110

To a solution of 1109 (0.010 mmol) in dichloromethane (2 mL) is added trichloroacetyl isocyanate (1.00 mmol). After 30 min, the reaction mixture is diluted with dichloromethane (4 mL) and neutral alumina (1 g) is added. The resultant suspension is stirred an additional 4 h. The reaction mixture is filtered and the concentrated filtrate is chromatographed on silica gel to afford 1110.

G. Arene analog 1111

A solution of 1110 (0.010 mmol) in 48% hydrofluoric acid-acetonitrile (1:9, 2 mL) is stirred at ambient temperature. After 12 h, saturated aqueous sodium bicarbonate (25 mL) is added and the mixture is extracted with ethyl acetate (3×20 mL). The combined organics are dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 1111.

EXAMPLE 62

Synthesis of Aldehyde 67

Enone (64)

To a -78° C. solution of aldehyde 27 (1.94 g, 6.13 mmol prepared from commercially available methyl (S)-(+)-3-hydroxy-2-methyl propionate generally according to Smith, et. al., J. Am. Chem. Soc. 1995, 117, 12011) in CH₂ Cl₂ (50 mL) was added (dropwise over 3 min) a -78° C. solution of TiCl₄ (0.68 mL, 6.18 mmol) in CH₂ Cl₂ (6 mL). The resultant solution was stirred an additional 3 min at -78° C. 4-Methyl-2-trimethylsiloxy- 1,3-pentadiene (1.89 g, 11.1 mmol, see Paterson, Tetrahedron Lett. 1979, 1519) was added dropwise over 2 min and the reaction mixture was further stirred at -78° C. for 2 h. A solution comprised of pH 8 phosphate buffer (100 mL) and saturated aqueous bicarbonate (50 mL) was added and the biphasic solution was warmed to ambient temperature, diluted with water (100 mL), and extracted with CH₂ Cl₂ (2×100 mL). The combined extracts were washed with saturated brine (75 mL), dried (MgSO₄) and concentrated. The residual oil was diluted with CH₂ Cl₂ /hexanes (1:1, 30 mL), cooled to 0° C. and treated with trichloroacetic acid (1.54 g, 9.42 mmol). After 5 h, the reaction mixture was diluted with hexanes (75 mL) and washed with water (2×50 mL), pH 8 phosphate buffer (50 mL) and saturated brine (50 mL) and was dried (MgSO₄) and concentrated in vacuo. Flash chromatography (hexanes/CH₂ Cl₂ /ethyl acetate, 12:4:1) afforded 64 (1.21 g, 56%) as a colorless oil: [α]_(D) ²³ -10.6°©0.88, CHCl₃); ¹ H NMR (500 MHZ, CDCl₃) d 6.09 (m, 1 H), 4.78 (ddd, J=10.0, 6.6, 4.3 Hz, 1 H), 3.65 (t, J=2.8 Hz, 1 H), 2.72 (dd, J=15.8, 4.3 Hz, 1 H), 2.66 (dd, J=15.8, 6.7 Hz, 1 H), 2.62 (qd, J=7.6, 3.2 Hz, 1 H), 2.13 (d, J=1.1 Hz, 3 H), 2.07 (dqd, J=10.0, 6.8, 2.4 Hz, 1 H), 1.87 (d, J=1.2 Hz, 3 H), 1.25 (d, J=7.6 Hz, 3 H), 0.97 (d, J=6.8 Hz, 3 H), 0.87 (s, 9 H), 0.05 (s, 3 H), 0.04 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 196.9, 173.6, 156.8, 124.1, 77.8, 74.3, 47.0, 43.9, 33.6, 27.7, 25.7, 20.9, 18.0, 16.1, 13.8, -4.5, -4.7.

Alcohol (65). A solution of enone 64 (109 mg, 0.307 mmol) in toluene (8 mL) was cooled to -95° C. and treated with K-Selectride (1.0 M in THF, 0.35 mL). After 2 h, glacial acetic acid (0.015 mL) was added and the resultant solution was warmed to ambient temperature and treated with pH 7 aqueous phosphate buffer solution (10 mL) and 30% aqueous hydrogen peroxide (0.5 mL). After 2 h, the aqueous layer was extracted with CH₂ Cl₂ (4×20 mL) and the combined organics were dried (MgSO₄) and concentrated. Flash chromatography (15% ethyl acetate/hexanes) afforded 65 (70 mg, 64%) as a colorless oil: ¹ H NMR (500 MHZ, CDCl₃) d 5.21 (apparent dt, J=8.6, 1.3 Hz, 1 H), 4.75 (br t, J=9.1 Hz, 1 H), 4.60 (td, J=9.9, 2.3 Hz, 1 H), 3.67 (t, J=3.0 Hz, 1 H), 2.66 (qd, J=7.5, 3.4 Hz, 1 H), 1.90 (dqd, 9.7, 6.8, 2.6 Hz, 1 H), 1.83 (ddd, J=14.5, 9.9, 2.4 Hz, 1 H), 1.71 (d, J=1.1 Hz, 3 H), 1.70 (d, J=1.2 Hz, 3 H), 1.65 (br s, 1 H), 1.60 (ddd, J=14.5, 10.1, 2.9 Hz, 1 H), 1.26 (d, J=7.6 Hz, 3 H), 0.99 (d, J=6.7 Hz, 3 H),0.89 (s, 9 H), 0.08 (s, 3 H), 0.07 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 174.0, 134.8, 127.7, 77.8, 74.2, 64.1, 43.7, 41.5, 34.6, 25.7, 25.6, 18.2, 17.9, 16.0, 13.7, -4.6, -4.8.

Silyl Ether (66). A solution of alcohol 65 (493 mg, 1.38 mmol) and imidazole (306 mg, 4.49 mmol) in DMF (6 mL) was cooled to 0° C. and treated with tert-butyldimethylsilyl chloride (386 mg, 2.56 mmol). The resultant solution was stirred 12 h at ambient temperature, diluted with ether (75 mL), washed with water (2×15 mL) and saturated brine (15 mL), dried over MgSO₄, and concentrated in vacuo. Flash chromatography (5% ethyl acetate/hexanes) afforded 66 (615 mg, 95%) as a colorless oil: ¹ H NMR (500 MHZ, CDCl₃) d 5.11 (apparent dt, J=8.6, 1.3 Hz, 1 H), 4.71 (ddd, 10.4, 8.7, 2.2 Hz, 1 H), 5.55 (td, J=10.4, 1.7 Hz, 1 H), 3.65 (t, J=2.7 Hz, 1 H), 2.63 (qd, J=7.6, 3.0 Hz, 1 H), 1.83 (dqd, 10.0, 6.8, 2.5 Hz, 1 H), 1.74 (ddd, J=14.2, 10.5, 1.8 Hz, 1 H), 1.68 (d, J=1.1 Hz, 3 H), 1.65 (d, J=1.2 Hz, 3 H), 1.44 (ddd, J=14.2, 10.6, 2.3 Hz, 1 H), 1.26 (d, J=7.6 Hz, 3 H), 0.98 (d, J=6.7 Hz, 3 H), 0.89 (s, 9 H), 0.85 (s, 9 H), 0.07 (s, 3 H), 0.06 (s, 3 H), 0.05 (s, 3 H), 0.01 (s, 3 H);

Aldehyde (67). A solution of olefin 66 (615 mg, 1.30 mmol) in CH₂ Cl₂ (20 mL) was cooled to -78° C. and treated with a stream of ozone and oxygen until the colorless solution became steel-blue in appearance. The reaction mixture was purged with a stream of air for 10 min, followed by the cautious addition of triphenylphosphine (375 mg, 1.42 mmol). The cooling bath was removed and the solution was stirred at ambient temperature for 1 h, concentrated, and chromatographed (20% ethyl acetate/hexanes) to afford 67 (486 mg, 84%) as a colorless oil that solidified upon standing at 0° C. ¹ H NMR (500 MHZ, CDCl₃) d 9.67 (br s, 1 H), 4.52 (td, J=10.5, 2.1 Hz, 1 H), 4.46 (dd, J=10.5, 3.5 Hz, 1 H), 3.67 (t, J=2.3 Hz, 1 H), 2.66 (qd, J=7.6, 2.6 Hz, 1 H), 1.95-1.84 (m, 3 H), 1.77 (ddd, J=14.1, 10.5, 2.1 Hz, 1 H), 1.27 (d, J=7.6 Hz, 3 H), 0.99 (d, J=6.7 Hz, 3 H), 0.92 (s, 9 H), 0.89 (s, 9 H), 0.13 (s, 3 H), 0.11 (s, 3 H), 0.08 (s, 3 H), 0.07 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 203.2, 173.1, 76.0, 74.7, 73.7, 44.2, 36.2, 34.1, 25.72, 25.66, 18.1, 17.9, 16.5, 14.0, -4.55, -4.63, -4.9, -5.2.

EXAMPLE 63

Synthesis of Phosphonium Salt (49) Employing Ultrahigh Pressure

Iodine (132 mg, 0.52 mmol) was added in one portion to a vigorously stirred solution of alcohol 40 (122 mg, 0.176 mmol, prepared from commercially available methyl (S)-(+)-3-hydroxy-2-methyl propionate generally according to Smith, et. al., J. Am. Chem. Soc. 1995, 117, 12011), PPh₃ (172 mg, 0.656 mmol) and imidazole (42 mg, 0.62 mmol) in benzene/ether (1:2, 1.5 mL) at 0° C. The resultant solution was stirred 1 h at 0° C. and 1 h at ambient temperature. The mixture was diluted with ether (10 mL), washed with saturated aqueous sodium metabisulfite (5 mL) and brine (10 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography afforded a colorless oil (147 mg, 100% yield). This material was combined with diisopropylethylamine (0.016 mL, 0.091 mmol), triphenylphosphine (152 mg, 0.58 mmol) and benzene/toluene (7:3, 1.0 mL) in a plastic syringe and subjected to a pressure of 12.8 Kbar. After 6 days, the reaction mixture was concentrated and chromatographed (10% MeCN/CHCl₃) to provide 49 [138 mg, 74% yield from 40] as a pale yellow foam: ¹ H NMR (500 MHZ, CDCl₃ ; concentration-dependent) d 7.82-7.76 (m, 15 H), 7.35 (d, J=8.8 Hz, 2 H), 6.84 (d, J=8.8 Hz, 2 H), 5.35 (s, 1 H), 5.30 (d, J=10.5 Hz, 1 H), 4.07 (dd, J=11.2, 4.7 Hz, 1 H), 3.77 (s, 3 H), 3.73-3.67 (m, 2 H), 3.56 (dd, J=7.0, 1.8 Hz, 1 H), 3.48 (dd, J=9.8, 1.7 Hz, 1 H), 3.46 (apparent t, J=11.1 Hz, 1 H), 3.31 (ddd, J=15.6, 11.2, 11.2 Hz, 1 H), 2.49 (ddq, J=10.5, 6.4, 6.4 Hz, 1 H), 2.25 (apparent t, J=12.1 Hz, 1 H), 2.10-1.92 (m, 3 H), 1. 85 (dqd, J=7.1, 7.1, 1.8 Hz, 1 H), 1.57-1.52 (m, 1 H), 1. 56 (s, 3 H), 0.98 (d, J=7.1 Hz, 3 H), 0.89 (d, J=6.6 Hz, 3 H), 0.852 (s, 9 H), 0.849 (s, 9 H), 0.72-0.71 (m, 3 H), 0.71 (d, J=6.6 Hz, 3 H), 0.69 (d, J=6.9 Hz, 3 H), 0.10 (s, 3 H), -0.02 (s, 3 H), -0.03 (s, 3 H), -0.07 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.8, 135.2 (d, J_(CP) =2.6 Hz), 133.5 (d, J_(CP) =10.0 Hz), 132.9, 131.4, 130.6 (d, J_(CP) =12.6 Hz), 130.3, 127.3, 118.4 (d, J_(CP) =85.5 Hz), 113.4, 101.0, 83.2, 80.1 (d, J_(CP) =14.0 Hz), 78.3, 73.2, 55.3, 38.1, 37.4, 36.0, 33.7 (d, J_(CP) =4.4 Hz), 33.6, 30.7, 26.1, 25.5 (d, J_(CP) =49.7 Hz), 22.9, 18.33, 18.29, 17.2, 17.1, 12.5, 12.1, 10.9, -3.2, -3.6, -3.7, -4.0; high resolution mass spectrum (FAB, NBA) m/z 937.5708 [(M-I)+; calcd for C₅₇ H₈₆ O₅ PSi₂ : 937.5751].

EXAMPLE 64

Synthesis of Diene (76)

Phosphonium salt 49 (166 mg, 0.156 mmol), was heated to 50° C. under vacuum (0.1 torr) for 18 h, dissolved in 0.8 mL of toluene, and cooled to 0° C. The resultant solution was treated with potassium bis(trimethylsilyl)amide (0.5 M in toluene, 0.32 mL), was stirred 20 min at 0° C. and 20 min at ambient temperature and re-chilled to -78° C. To this reaction mixture was transferred via cannula a solution of aldehyde 67 (58 mg, 0.13 mmol) in toluene (0.3 mL+2×0.2 mL rinse). The resultant solution was allowed to slowly warm to -20° C. during 1 h. A solution of pH 7 phosphate buffer was added and the biphasic solution was warmed to ambient temperature and extracted with CH₂ Cl₂ (4×20 mL). The combined organics were dried (MgSO₄), concentrated, and chromatographed (10% ethyl acetate/hexanes) to afford 76 (83 mg, 57%) as a colorless oil that solidified upon standing: [α]_(D) ²³ +32.1°©0.68, CHCl₃); ¹ H NMR (500 MHZ, CDCl₃) d 6.97 (br d, J=8.7 Hz, 2 H), 6.87 (br d, J=8.7 Hz, 2 H), 5.34 (s, 1 H), 5.29 (dd, J=11.1, 7.8 Hz, 1 H), 5.19 (t, J=10.6 Hz, 1 H), 5.07 (d, J=10.0 Hz, 1 H), 4.78 (br t, J=9.1 Hz, 1 H), 4.52 (br t, J=10.0 Hz, 1 H), 4.10 (dd, J=11.1, 4.6 Hz, 1 H), 3.80 (s, 3 H), 3.64 (m, 2 H), 3.54-3.46 (m, 2 H), 3.25 (t, J=5.3 Hz, 1 H), 2.65-2.57 (m, 2 H), 2.51 (m, 1 H), 2.31 (t, J=12.2 Hz, 1 H), 2.06 (m, 1 H), 1.96 (m, 1 H), 1.90 (dqd, J=7.1, 7.0, 1.5 Hz, 1 H), 1. 78 (ddd, J=10.3, 6.6, 2.1 Hz, 1 H), 1.72 (ddd, J=14.0, 11.0, 1.5 Hz, 1 H), 1.67 (br d, J=11.6 Hz, 1 H), 1.56 (m, 1 H), 1.55 (s, 3 H), 1.20 (d, J=7.6 Hz, 3 H), 1.02 (d, J=7.1 Hz, 3 H), 0.92 (s, 9 H), 0.91 (s, 9 H), 0.90 (d, J=7.0 Hz, 3 H), 0.96 (d, J=6.8 Hz, 3 H), 0.95 (d, J=6.7 Hz, 3 H), 0.89 (s, 9 H), 0. 87 (s, 9 H), 0.75 (d, J=6.9 Hz, 3 H), 0.74 (d, J=6.7 Hz, 3 H), 0. 073 (s, 3 H), 0.071 (s, 3 H), 0.06 (s, 6 H), 0.05 (s, 6 H), 0.01 (s, 3 H), 0.00 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 173.2, 159.8, 133.6, 132.4, 131.9, 131.5, 131.4, 127.3, 113.4, 101.0, 83.4, 80.4, 78.4, 76.9, 74.9, 73.3, 64.7, 55.2, 44.1, 42.7, 38.0, 37.4, 35.2, 34.2, 34.0, 30.8, 26.3, 26.2, 25.9, 25.7, 23.2, 18.43, 18.39, 18.1, 17.9, 17.1, 16.4, 16.2, 14.0, 12.8, 12.1, 10.8, -2.9, -3.5, -3.8, -4.37, -4.41, -4.5, -4.87, -4.88. Recrystallization from hexanes afforded fine needles: mp 117-119° C.

EXAMPLE 65

Synthesis of Aldehyde (77).

A solution of acetal 76 (20 mg, 0.018 mmol) in CH₂ Cl₂ (2 mL) was cooled to -78° C. and diisobutylaluminum hydride (1.0 M in toluene, 0.18 mL, 0.18 mmol) was added over 5 min. After an additional 10 min at -78° C. and 30 min at 0° C., the reaction was quenched with saturated aqueous potassium sodium tartrate (0.5 mL). The mixture was then diluted with ether (20 mL), washed with saturated aqueous potassium sodium tartrate and brine (10 mL each), dried over MgSO₄, filtered and concentrated. Flash chromatography (10% ethyl acetate/hexanes) provided an epimeric mixture of hydroxy-lactols (14.7 mg, 74% yield) as a colorless oil. The mixture of lactols (14.7 mg, 0.0133 mmol) in CH₂ Cl₂ (2 mL) was cooled to 0° C. and treated with pyridinium dichromate (26 mg, 0.069 mmol). The reaction mixture was stirred 12 h at ambient temperature, diluted with ethyl acetate (10 mL), filtered (Celite) and concentrated. Flash chromatography (10% ethyl acetate/hexanes) afforded 77 (12.4 mg, 62% from 76) as a colorless oil: ¹ H NMR (500 MHZ, CDCl₃) d 9.80 (d, J=2.4 Hz, 1 H), 7.22 (br d, J=8.6 Hz, 2 H), 6.86 (br d, J=8.6 Hz, 2 H), 5.30 (dd, J=11.1, 7.9 Hz, 1 H), 5.20 (dd, J=10.9, 10.1 Hz, 1 H), 5.11 (d, J=10.0 Hz, 1 H), 4.79 (apparent t, J=9.2 Hz, 1 H), 4.52 (br t, J=9.6 Hz, 1 H), 4.47 (s, 2 H), 3.80 (s, 3 H), 3.62 (t, J=2.5 Hz, 1 H), 3.59 (m, 2 H), 3.26 (t, J=5.3 Hz, 1 H), 2.75 (m, 1 H), 2.62 (m, 2 H), 2.50 (m, 1 H), 2.24 (t, J=12.4 Hz, 1 H), 1.99-1.88 (m, 2 H), 1.83-1.65 (m, 3 H), 1.59 (s, 3 H), 1.58 (m, 1 H), 1.21 (d, J=7.6 Hz, 3 H), 1.13 (d, J=7.0 Hz, 3 H), 1.04 (d, J=7.0 Hz, 3 H), 0.96 (d, J=6.8 Hz, 3 H), 0.95 (d, J=6.9 Hz, 3 H), 0.94 (s, 9H), 0.91 (s, 9 H), 0.89 (d, J=6.9 Hz, 3 H), 0.88 (s, 9 H), 0.87 (s, 9 H), 0.75 (d, J=6.8 Hz, 3 H), 0.09 (s, 3 H), 0.08 (s, 3 H), 0.07 (s, 3 H), 0.06 (s, 6 H), 0.05 (s, 6 H), 0.01 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 204.5, 173.2, 159.3, 133.5, 132.5, 132.3, 130.8, 130.3, 129.1, 113.8, 82.6, 80.4, 76.9, 74.9, 74.4, 64.6, 55.3, 49.5, 44.1, 42.7, 40.3, 37.4, 36.8, 35.2, 35.0, 34.2, 26.3, 26.2, 25.9, 25.7, 23.1, 18.5, 18.4, 18.1, 17.9, 17.1, 16.4, 16.2, 14.1, 13.4, 12.2, 11.4, -3.0, -3.3, -3.4, -4.3, -4.4, -4.5, -4.9.

EXAMPLE 66

Synthesis of Tetraene (58)

Method A. A solution of allyldiphenylphosphine (0.0035 mL, 0.0162 mmol) in anhydrous THF was cooled to -78° C. and t-BuLi (1.7 M in pentane, 0.010 mL, 0.017 mmol) was added. The mixture was stirred at 0° C. for 30 min, recooled to -78° C. and treated Ti(OiPr)₄ (0.005 mL, 0.017 mmol). After 30 min, a cold (-78° C.) solution of the aldehyde 77 (3.5 mg, 0.0032 mmol) in THF (0.25 mL +0.25 mL rinse) was introduced via cannula, and the mixture was stirred 10 min further at -78° C. and at 0° C. for 30 min. Methyl Iodide (0.0025 mL, 0.04 mmol) was then added, and the reaction was warmed to room temperature and stirred overnight. The reaction mixture was diluted with ether (10 mL), washed with 1.0 M aqueous NaHSO₄ and brine (5 mL each), dried over MgSO₄, filtered and concentrated in vacuo. Flash chromatography (2% ethyl acetate/hexane) gave a 1.2:1 mixture of Z/E isomers (2.1 mg, 58%) as an oil. Pipette flash chromatography on 10% silver nitrate-silica gel (5% ether/hexanes) furnished the Z-olefin 58 as a colorless oil: ¹ H NMR (500 MHZ, CDCl₃) d 7.25 (d, J=8.2 Hz, 2 H), 6.84 (d, J=8.7 Hz, 2 H), 6.57 (dddd, J=16.8, 11.0, 11.0, 0.7 Hz, 1 H), 6.00 (apparent t, J=11.1 Hz, 1 H), 5.55 (apparent t, J=10.5 Hz, 1 H), 5.26 (dd, J=11.2, 7.8 Hz, 1 H), 5.20-5.16 (m, 2 H), 5.09 (d, J=10.1 Hz, 1 H), 5.05 (d, J=2.2 Hz, 1 H), 5.03 (d, J=10.0 Hz, 1 H), 4.67 (apparent t, J=9.1 Hz, 1 H), 4.49 (AB_(q), J_(AB) =10 .6 Hz, Δγ_(AB) =41.3 Hz, 2 H), 3.78 (s, 3 H), 3.68 (apparent t, J=10.2 Hz, 1 H), 3.52 (apparent t, J=2.6 Hz, 1 H), 3.43 (dd, J=4.8, 3.9 Hz, 1 H), 3.24-3.21 (m, 2 H), 3.01-2.94 (m, 1 H), 2.67 (dq, J=12.8, 7.4 Hz, 1 H), 2.61 (dq, J=12.8, 7.5 Hz, 1 H), 2.71-2.57 (m, 1 H), 2.46-2.39 (m, 1 H), 2.00 (apparent t, J=12.4 Hz, 1 H), 1.83-1.73 (m, 3 H), 1.64 (br d, J=14.0 Hz, 1 H), 1.62-1.52 (m, 2 H), 1.55 (d, J=0.5 Hz, 3 H), 1.36 (ddd, J=13.7, 10.8, 1.5 Hz, 1 H), 1.26 (d, J=7.4 Hz, 3 H), 1.25 (d, J=7.4 Hz, 3 H), 1.08 (d, J=6.8 Hz, 3 H), 0.98 (d, J=6.8 Hz, 3 H), 0.94 (d, J=7.1 Hz, 3 H), 0. 93 (s, 9 H), 0.90 (s, 9 H), 0.89 (s, 9 H), 0.89-0.86 (m, 3 H), 0.86 (s, 9 H), 0.73 (d, J=6.8 Hz, 3 H), 0.70 (d, J=6.7 Hz, 3 H), 0.08 (s, 6 H), 0.05 (s, 3 H), 0.02 (s, 3 H), 0.013 (s, 3 H), 0.010 (s, 6 H), -0.02 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.1, 134.5, 134.3, 132.2, 131.9, 131.8, 131.2, 129.13, 129.07, 117.6, 113.7, 84.6, 80.9, 80.5, 76.5, 75.0, 74.2, 65.5, 55.3, 42.5, 41.9, 40.2, 37.2, 36.1, 35.4, 35.3, 34.5, 29.7, 26.3, 26.0, 25.9, 25.1, 23.1, 18.7, 18.6, 18.5, 18.14, 18.09, 17.0, 16.8, 15.6, 14.8, 14.4, 11.6, 10.6, -2.8, -3.2, -3.3, -3.6, -4.2, -4.5, -4.90, -4.93; high resolution mass spectrum (FAB, NBA) m/z 1195.8001 [(M+Na)⁺ ; calcd for C₆₆ H₁₂₄ O₇ SSi₄ Na: 1195.8042].

Method B. A vigorously stirred suspension of chromium(III) chloride (7.8 mg, 0.048 mmol) in anhydrous THF (0.6 mL) was cooled to 0° C. and treated with lithium aluminum hydride (1.0 M in ether, 0.022 mL, 0.022 mmol). The resultant solution was stirred 20 min at room temperature and re-cooled to 0° C. Aldehyde 77 (3.9 mg, 0.035 mmol) was added in THF (0.4 mL). After 10 min, a mixture of 3-bromo-1-trimethylsilyl-1-propene and 3-bromo-3-trimethlsilyl-1-propene (3:1, 0.002 mL, 0.01 mmol, see, Hodgson, et. al., Tetrahedron Lett. 1992, 33, 4761) was added. The reaction mixture was stirred at ambient temperature for 12 h and then diluted with hexanes-ethyl acetate (9:1), washed with water, saturated aqueous sodium bicarbonate and brine, dried over MgSO₄ and concentrated. Flash chromatography afforded a 2.8:1 mixture of hydroxy silanes (3.8 mg, 89%). The mixture was dissolved in THF (0.6 mL), cooled to 0° C. and treated with potassium bis(trimethylsilyl)amide (0.5 M in toluene, 0.068 mL, 0.34 mmol). After 15 min, trichloroacetic acid (5 mg, 0.03 mmol) was added and the reaction mixture was diluted with hexanes and washed with water and brine. The combined aqueous washings were further extracted with hexanes. The combine organics were dried over MgSO₄ and concentrated in vacuo. Flash Chromatography afforded (2.6 mg, 65% yield for 2 steps) of tetraene 58 as a colorless oil.

Method C. Phosphonium salt 75 (120 mg, 0.11 mmol) was heated to 50° C. under vacuum (0.1 torr) for 18 h and dissolved in 0.4 mL of anhydrous toluene. The resultant solution was cooled to 0° C. and was treated with potassium bis(trimethylsilyl)amide (0.5 M in toluene, 0.23 mL, 0.115 mmol). The resultant solution was stirred 20 min at 0° C. and 20 min at ambient temperature before being chilled to -78° C. Aldehyde 67 (46 mg, 0.10 mmol) was added in toluene (0.4 mL) and the reaction mixture was allowed to warm to 0° C. during 2.5 h. The reaction was partitioned between hexanes (10 mL) and pH 7 phosphate buffer solution(10 mL). The aqueous layer was extracted with CH₂ Cl₂ (4×15 mL) and the combined organics were dried over MgSO₄ and concentrated. Flash chromatography afforded tetraene 58 (49 mg, 42% yield).

EXAMPLE 67

Synthesis of Alcohol (71)

A solution of (+)-39 (106 mg, 0.13 mmol, prepared from commercially available methyl (S)-(+)-3-hydroxy-2-methyl propionate generally as described by Smith, et. al., J. Am. Chem. Soc. 1995, 117, 12011)) in CH₂ Cl₂ was cooled to 0° C. and treated with neat diisobutylaluminum hydride (0.15 mL, 0.84 mmol). After 1 h, a solution of saturated aqueous potassium sodium tartrate (10 mL) was added (dropwise until cessation of hydrogen evolution) and the resultant biphasic mixture was stirred 4 h at ambient temperature. The aqueous layer was extracted with CH₂ Cl₂ (3×10 mL) and the combined organics were dried over MgSO₄ and concentrated in vacuo. Flash chromatography (15% ethyl acetate/hexanes) afforded alcohol 71 (88 mg, 83%) as a colorless oil: ¹ H NMR (500 MHZ, CDCl₃) d 7.26-7.20 (m, 4 H), 6.87-6.82 (m, 4 H), 5.03 (br d, J=10.2 Hz, 1 H), 4.50 (AB_(q), J=10.5 Hz, Dv=12.1 Hz, 2 H), 4.37 (AB_(q), J=11.6 Hz, Dv=14.2 Hz, 2 H), 3.78 (s, 3 H), 3.77 (s, 3 H), 3.74 (m, 1 H), 3.57 (quintet, J=10.5 Hz, 1 H), 3.51 (dd, J=5.1, 3.7 Hz, 1 H), 3.47 (dd, J=9.1, 4.9 Hz, 1 H), 3.38 (dd, J=6.0, 4.6 Hz, 1 H), 3.35 (t, J=5.5 Hz, 1 H), 3.20 (t, dd, J=8.9, 8.6 Hz, 1 H), 2.68 (br t, J=5.5 Hz, 1 H), 2.51 (m, 1 H), 2.22 (br t, J=12.4 Hz, 1 H), 2.00-1.84 (m, 4 H), 1.74 (br d, J=12.5 Hz, 1 H), 1.58 (d, J=0.9 Hz, 3 H), 1.04 (d, J=7.3 Hz, 3 H), 1.02 (d, J=7.2 Hz, 3 H), 0.93 (d, J=7.0 Hz, 3 H), 0.92 (s, 9 H), 0.88 (d, J=6.9 Hz, 3 H), 0.87 (s, 9 H), 0.07 (s, 3 H), 0.06 (s, 3 H), 0.02 (s, 3 H), 0.1 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 159.4, 159.0, 131.64, 131.60, 131.0, 130.4, 129.3, 129.0, 113.9, 113.7, 86.2, 78.4, 77.5, 75.2, 72.7, 72.6, 65.4, 55.3, 39.9, 38.7, 37.5, 36.7, 35.7, 35.2, 26.2, 26.1, 23.1, 18.5, 18.4, 17.0, 15.7, 14.6, 13.7, 11.4, -3.3, -3.4, -3.9.

EXAMPLE 68

Synthesis of Aldehyde (72)

A solution of alcohol 71 (88 mg, 0.108 mmol) and triethylamine (0.075 mL, 0.54 mmol) in CH₂ Cl₂ (2 mL) and dimethylsulfoxide (1 mL) was treated with sulfur trioxide-pyridine (55 mg, 0.34 mmol). After 90 min, the mixture was diluted with ether (30 mL), washed with water (10 mL), aqueous NaHSO₄ (0.1 M, 10 mL) and brine (10 mL), dried over MgSO₄, filtered and concentrated. Flash chromatography (5% ethyl acetate/hexanes) afforded 72 (84 mg, 96% yield) as a colorless oil: ¹ H NMR (500 MHZ, CDCl₃) d 9.79 (d, J=2.4 Hz, 1 H), 7.24-7.18 (m, 4 H), 6.87-6.82 (m, 4 H), 5.03 (br d, J=10.2 Hz, 1 H), 4.46 (AB_(q), J=10.8 Hz, Dv=7.1 Hz, 2 H), 4.37 (AB_(q), J=11.6 Hz, Dv=14.0 Hz, 2 H), 3.78 (s, 3 H), 3.77 (s, 3 H), 3.57 (m, 2 H), 3.47 (dd, J=9.1, 5.0 Hz, 1 H), 3.39 (dd, J=5.9, 4.7 Hz, 1 H), 3.21 (t, J=8.7 Hz, 1 H), 2.73 (m, 1 H), 2.51 (m, 1 H), 2.25 (t, J=12.4 Hz, 1 H), 1.99-1.86 (m, 3 H), 1.70 (br d, J=12.4 Hz, 1 H), 1.58 (s, 3 H), 1.12 (d, J=7.0 Hz, 3 H), 1.03 (d, J=7.0 Hz, 3 H), 0.93 (d, J=7.0 Hz, 3 H), 0.92 (s, 9 H), 0.88 (d, J=6.9 Hz, 3 H), 0.87 (s, 9 H), 0.74 (d, J=6.8 Hz, 3 H), 0.07 (s, 3 H), 0.06 (s, 3 H), 0.02 (s, 3 H), 0.01 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 204.5, 159.3, 159.0, 131.7, 131.5, 131.0, 130.3, 129.1, 129.0, 113.8, 113.7, 82.6, 78.4, 77.2, 74.4, 72.7, 72.5, 55.25, 55.24, 49.5, 40.3, 38.7, 36.7, 35.7, 35.0, 26.2, 26.1, 23.1, 18.5, 18.4, 17.0, 14.6, 13.4, 12.2, 11.4, -3.3, -3.4, -3.89, -3.91.

EXAMPLE 69

Synthesis of Triene (73)

A solution lithium aluminum hydride (1.0 M in ether, 0.022 mL, 0.022 mmol).was added dropwise to a vigorously stirred suspension of chromium(III) chloride (40 mg, 0.25 mmol) in anhydrous THF (2 mL) at 0° C. The resultant solution was stirred 45 min at room temperature and re-cooled to 0° C. Aldehyde 72 (50 mg, 0.061 mmol) was added in THF (3 mL) via cannula. After 10 min, a mixture of 3-bromo-1-trimethylsilyl-1-propene and 3-bromo-3-trimethlsilyl-1-propene (3:1, 0.025 mL, 0.13 mmol) was added. The reaction mixture was further stirred 30 min at 0° C. and at ambient temperature for 12 h. Methanol (1 mL) and aqueous potassium hydroxide solution (6 M, 2 mL) were added and the resultant solution was stirred 1 h at ambient temperature. The aqueous layer was extracted with hexanes (3×15 mL). The combined organics were washed with brine, dried over MgSO₄ and concentrated. Flash chromatography provided triene 73 (47 mg, 92%) as a single geometric isomer: ¹ H NMR (500 MHZ, CDCl₃) d 7.27-7.20 (m, 4 H), 6.87-6.82 (m, 4 H), 6.57 (dt, J=16.8, 10.4 Hz, 1 H), 6.00 (t, J=11.0 Hz, 1 H), 5.55 (t, J=10.5 Hz, 1 H), 5.18 (dd, J=16.8, 1.6 Hz, 1 H), 5.09 (d, J=10.1 Hz, 1 H), 4.96 (d, J=10.2 Hz, 1 H), 4.50 (AB_(q), J=10.6 Hz, Dv=43.6 Hz, 2 H), 4.36 (AB_(q), J=11.6 Hz, Dv=16.9 Hz, 2 H), 3.78 (s, 3 H), 3.77 (s, 3 H), 3.44 (m, 2 H), 3.36 (dd, J=6.4, 4.4 Hz, 1 H), 3.24 (dd, J=7.4, 3.7 Hz, 1 H), 3.19 (t, J=8.8 Hz, 1 H), 2.98 (m, 1 H), 2.44 (m, 1 H), 2.03 (t, J=12.4 Hz, 1 H), 1.95 (m, 1 H), 1.84-1.72 (m, 2 H), 1.65 (br d, J=11.4 Hz, 1 H), 1.52 (s, 3 H), 1.09 (d, J=6.8 Hz, 3 H), 0.99 (d, J=6.9 Hz, 3 H), 0.93 (s, 9 H), 0.91 (d, J=7.0 Hz, 3 H), 0.87 (s, 9 H), 0.85 (d, J=6.6 Hz, 3 H), 0.70 (d, J=6.7 Hz, 3 H), 0.09 (s, 3 H), 0.08 (s, 3 H), 0.01 (s, 6 H); 13C NMR (125 MHZ, CDCl₃) d 159.1, 159.0, 134.5, 132.2, 131.8, 131.2, 131.1, 129.1, 129.0, 117.6, 113.7, 84.6, 78.4, 77.2, 75.0, 72.7, 72.5, 55.3, 40.1, 38.9, 36.1, 35.5, 35.4, 26.3, 26.1, 23.0, 18.7, 18.6, 18.4, 17.2, 14.7, 14.4, 10.6, -3.2, -3.3, -3.89, -3.92.

EXAMPLE 70

Synthesis of Alcohol (74)

Method A: Bis-ether 73 is dissolved in a mixture of CH₂ Cl₂ and water (19:1) and cooled to 0° C. 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (1 eq) is added and the resultant solution is stirred 2 h at 0° C. The reaction mixture is diluted with hexanes and washed with aqueous sodium hydroxide solution, dried over MgSO₄ and concentrated. Flash chromatography affords 74.

Method B: A solution of 73 and ethanethiol in CH₂ Cl₂ is cooled to -78° C. and treated with a Lewis acid (e.g. magnesium bromide, borontrifluoride etherate, tin(IV) chloride, titanium(IV) chloride, etc.). The resultant solution is allowed to slowly warm until reaction ensues. The reaction is then quenched with aqueous sodium hydroxide solution, washed with water and brine, dried over MgSO₄, concentrated and chromatographed to afford 74: ¹ H NMR (500 MHZ, CDCl₃) d 7.27 (br d, J=8.6 Hz, 2 H), 6.87 (br d, J=8.6 Hz, 2 H), 6.60 (dt, J=16.8, 10.5 Hz, 1 H), 6.04 (t, J=11.0 Hz, 1 H), 5.57 (t, J=10.5 Hz, 1 H), 5.55 (dd, J=16.8, 1.8 Hz, 1 H), 5.12 30 (d, J=10.3 Hz, 1 H), 4.97 (d, J=10.2 Hz, 1 H), 4.51 (AB_(quartet), J=10.6 Hz, Dv=47.6 Hz, 2 H), 3.80 (s, 3 H), 3.66 (dt, J=10.9, 4.3 Hz, 1 H), 3.50 (m, 1 H), 3.44 (dd, J=4.8, 4.0 Hz, 1 H), 3.39 (dd, 6.9, 3.8 Hz, 1 H), 3.25 (dd, J=7.4, 3.7 Hz, 1 H), 3.00 (m, 1 H), 2.54 (m, 1 H), 2.31 (br t, J=5.5 Hz, OH), 2.05 (t, J=12.4 Hz, 1 H), 1.85-1.73 (m, 3 H), 1.67 (br d, J=13.4 Hz, 1 H), 1,56 (s, 3 H), 1.11 (d, J=6.8 Hz, 3 H), 1.00 (d, J=7.0 Hz, 3 H), 0.99 (d, J=7.0 Hz, 3 H), 0.95 (s, 9 H), 0.92 (s, 9 H), 0.91 (d,=6.6 Hz, 3 H), 0.72 (d, J=6.7 Hz, 3 H), 0.10 (s, 9 H), 0.07 (s, 3 H).

EXAMPLE 71

Synthesis of Phosphonium Salt (75)

Iodine (127 mg, 0.50 mmol) was added in one portion to a vigorously stirred solution of alcohol 74 (120 mg, 0.167 mmol), triphenylphosphine (156 mg, 0.595 mmol), and imidazole (40 mg, 0.59 mmol) in benzene/ether (1:1) at -10° C. The resultant solution was stirred 30 min at -10° C. and 30 min at ambient temperature, was diluted with 30 mL hexanes and was washed with water (2×10 mL), saturated aqueous sodium metabisulfite (10 mL), saturated aqueous sodium bicarbonate (10 mL) and saturated brine (10 mL), dried over MgSO₄ and concentrated. Flash chromatography (2% ether/hexanes) provided a colorless oil. The oil was combined with diisopropylethylamine (0.015 mL, 0.086 mmol), triphenylphosphine (199 mg, 0.758 mmol), and benzene/toluene (7:3, 1.0 mL) in a plastic syringe and was subjected to a pressure of 12.8 Kbar. After 16 days, the reaction mixture was concentrated and chromatographed (10% acetonitrile/chloroform) to afford phosphonium salt 75 (126 mg, 76% for two steps) as a pale yellow film: ¹ H NMR (500 MHZ, CDCl₃) d 8.84-7.65 (m, 15 H), 7.27 (br d, J=8.6 Hz, 2 H), 6.87 (br d, J=8.6 Hz, 2 H), 6.54 (dt, J=16.8, 10.5 Hz, 1 H), 5,89 (t, J=11.0 Hz, 1 H), 5.51 (t, J=10.5 Hz, 1 H), 5.30 (d, J=10.5 Hz, 1 H), 5.21 (d, J=16.8, 1 H), 5.08 (d, J=10.2 Hz, 1 H), 4.51 (AB_(q), J=10.4 Hz, Dv=55.6 Hz, 2 H), 3.78 (s, 3 H), 3.76-3.68 (m, 2 H), 3.42 (dd, J=5.4, 3.1 Hz, 1 H), 3.25-3.17 (m, 2 H), 2.97 (m, 1 H), 2.41 (m, 1 H), 2.06 (m, 1 H), 1.95 (t, J=12.3 Hz, 1 H), 1.77-1.72 (m, 2 H), 1.58 (br d, J=11.9 Hz, 1 H), 1.53 (s, 3 H), 1.10 (d, J=6.8 Hz, 3 H), 0.96 (d, J=6.8 Hz, 3 H), 0.91 (s, 9 H), 0.89 (d, J=7.0 Hz, 3 H), 0.86 (s, 9 H), 0.69 (d, J=6.9 Hz, 3 H), 0.66 (d, J=6.7 Hz, 3 H), 0.09 (s, 3 H), 0.08 (s, 3 H), 0.04 (s, 3 H), -0.05 (s, 3 H).

EXAMPLE 72

Synthesis of Alcohol (+)-59

At 0° C., a solution of PMB ether (+)-58 (4.0 mg, 3.55 mmol) in CH₂ Cl₂ (0.5 mL) was treated with H₂ O (50 mL) and DDQ (3.0 mg, 13.2 mmol). The mixture was stirred for 1 h and then diluted with ethyl acetate (30 mL), washed with brine (3×30 mL), dried over MgSO₄, filtered and concentrated. Pipette flash chromatography (2% ethyl acetate/hexanes) provided 59 (3.4 mg, 95% yield) as a colorless oil: ¹ H NMR (500 MHZ, CDCl₃) d 6.61 (ddd, J=16.8, 10.9, 10.9 Hz, 1 H), 6.13 (apparent t, J=11.0 Hz, 1 H), 5.32 (apparent t, J=10.5 Hz, 1 H), 5.28 (dd, J=11.1, 7.9 Hz, 1 H), 5.24-5.21 (m, 1 H), 5.19 (apparent t, J=10.3 Hz, 1 H), 5.14 (d, J=10.2 Hz, 1 H), 5.06 (d, J=10.0 Hz, 1 H), 4.76 (apparent t, J=9.3 Hz, 1 H), 4.50 (apparent t, J=9.9 Hz, 1 H), 3.62 (apparent t, J=2.4 Hz, 1 H), 3.60 (dd, J=5.5, 3.4 Hz, 1 H), 3.32 (br d, J=5.3 Hz, 1 H), 3.24 (apparent t, J=5.1 Hz, 1 H), 2.79 (ddq, J=9.9, 6.7, 6.7 Hz, 1 H), 2.60 (qd, J=7.6, 2.7 Hz, 1 H), 2.63-2.57 (m, 1 H), 2.50-2.45 (m, 1 H), 2.16 (apparent t, J=12.3 Hz, 1 H), 1.90-1.77 (m, 3 H), 1.75-1.69 (m, 2 H), 1.57 (s, 3 H), 1.60-1.50 (m, 1 H), 1.20 (d, J=7.6 Hz, 3 H), 0. 96 (d, J=6.8 Hz, 3 H), 0.95 (d, J=6.6 Hz, 3 H), 0.95-0.93 (m, 6 H), 0.91 (s, 9 H), 0.89 (s, 9 H), 0.89-0.84 (m, 3 H), 0.87 (s, 9 H), 0.85 (s, 9 H), 0.73 (d, J=6.8 Hz, 3 H), 0.07 (apparent s, 6 H), 0.052 (s, 3 H), 0.051 (s, 3 H), 0.04 (apparent s, 6 H), 0.03 (s, 3 H), -0.01 (s, 3 H); 13C NMR (125 MHZ, CDCl₃) d 173.3, 134.7, 133.5, 132.5, 132.1, 132.0, 131.5, 131.0, 118.4, 80.5, 78.8, 76.4, 74.9, 64.7, 44.1, 42.7, 38.0, 37.4, 36.3, 36.1, 35.2, 35.1, 34.2, 26.3, 26.2, 25.9, 25.7, 23.2, 18.5, 18.1, 18.0, 17.3, 17.2, 16.4, 16.1, 14.1, 13.7, 9.4, -3.0, -3.3, -3.6, -4.34, -4.36, -4.5, -4.8; high resolution mass spectrum (FAB, NBA) m/z 1029.7273 [(M+Na)⁺ ; calcd for C₅₆ H₁₁₀ O₇ Si₄ Na: 1029.7226].

example 73

Synthesis of Carbamate (+)-60

A solution of alcohol 59 (2.2 mg, 2.19 mmol) in CH₂ Cl₂ (0.5 mL) was treated with trichloroacetyl isocyanate (20 mL, 0.17 mmol) at room temperature for 30 min. CH₂ Cl₂ (2.0 mL) and neutral alumina (500 mg) were then added and the mixture was stirred at room temperature for 2 h, filtered through a short plug of silica, and concentrated. Pipette flash chromatography (10% ethyl acetate/hexane) furnished 60 (1.9 mg, 83% yield) as a colorless oil: IR (film, NaCl) 3510 (m), 3360 (m, br), 3180 (m), 2960 (s), 2930 (s), 2880 (s), 2855 (s), 1730 (s, br), 1596 (m), 1460 (s), 1385 (s), 1362 (s), 1325 (m), 1255 (s), 1220 (m), 1100 (s), 1043 (s), 983 (m), 937 (m), 904 (m), 832 (s), 770 (s), 663 (m) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 6.58 (dddd, J=16.8, 10.6, 10.6, 0.7 Hz, 1 H), 6.01 (apparent t, J=11.0 Hz, 1 H), 5.36 (apparent t, J=10.4 Hz, 1 H), 5.27 (dd, J=11.1, 7.9 Hz, 1 H), 5.22-5.16 (m, 2 H), 5.12 (d, J=10.1 Hz, 1 H), 5.03 (d, J=10.0 Hz, 1 H), 4.76 (apparent t, J=9.2 Hz, 1 H), 4.71 (apparent t, J=6.1 Hz, 1 H), 4.50 (ddd, J=10.5, 10.5, 1.3 Hz, 1 H), 4.44 (br s, 2 H), 3.62 (apparent t, J=2.4 Hz, 1 H), 3.42 (apparent t, J=4.5 Hz, 1 H), 3.22 (apparent t, J=5.3 Hz, 1 H), 2.98 (ddq, J=10.1, 6.6, 6.6 Hz, 1 H), 2.60 (qd, J=7.6, 2.7 Hz, 1 H), 2.63-2.55 (m, 1 H), 2.48-2.41 (m, 1 H), 2.09 (apparent t, J=12.4 Hz, 1 H), 1. 93-1.88 (m, 1 H), 1.87-1.77 (m, 2 H), 1.71 (ddd, J=14.1, 10.8, 1.6 Hz, 1 H), 1.67 (br d, J=13.7 Hz, 1 H), 1.56 (apparent s, 3 H), 1.55-1.50 (m, 1 H), 1.21 (d, J=7.6 Hz, 3 H), 0.98 (d, J=6.8 Hz, 3 H), 0.95 (d, J=7.0 Hz, 3 H), 0.94 (d, J=7.5 Hz, 3 H), 0.918 (d, J=6.8 Hz, 3 H), 0.915 (s, 9 H), 0.89 (s, 9 H), 0.86 (s, 9 H), 0.853 (d, J=6.4 Hz, 3 H), 0.847 (s, 9 H), 0.70 (d, J=6.8 Hz, 3 H), 0.09 (s, 3 H), 0.07 (s, 3 H), 0.053 (s, 3 H), 0.051 (s, 3 H), 0.040 (s, 3 H), 0.037 (s, 3 H), 0.03 (s, 3 H), -0.02 (s, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 173.3, 156.9, 133.6, 133.5, 132.4, 132.1, 131.9, 131.4, 129.8, 118.0, 80.5, 78.9, 74.9, 64.6, 44.2, 42.7, 37.8, 37.4, 36.0, 35.3, 35.2, 34.5, 34.2, 26.3, 26.2, 25.9, 25.7, 23.0, 18.5, 18.4, 18.1, 18.0, 17.5, 17.1, 16.44, 16.38, 14.1, 13.7, 10.1, -3.0, -3.4, -3.6, -4.4, -4.5, -4.8; high resolution mass spectrum (FAB, NBA) m/z 1072.7264 [(M+Na)⁺ ; calcd for C₅₇ H₁₁₁ NO₈ Si₄ Na: 1072.7283 ].

EXAMPLE 74

Synthesis of (+)-Discodermolide.

Tetrasilyl derivative (+)-60 (5.8 mg, 5.5 mmol) was dissolved in 48% HF--CH₃ CN (1:9, 1.0 mL) at room temperature. After 12 h, the reaction mixture was quenched with saturated aqueous NaHCO₃ (5 mL) and extracted with ethyl acetate (3×10 mL). The combined extracts were washed with brine (5 mL), dried over MgSO₄, filtered and concentrated. Pipette flash chromatography (gradient elution; 1:30→1:6 MeOH/CHCl₃) gave (+)-1 (2.0 mg, 60% yield) as a white amorphous solid: [α]_(D) ²³ +15 °©0.033, MeOH); IR (CHCl₃) 3690 (w), 3620 (w), 3540 (w), 3430 (w), 3020 (s), 2975 (m), 2935 (m), 1740 (m), 1590 (w), 1540 (w) , 1520 (w) , 1467 (w) , 1430 (w) , 1385 (m) , 1330 (w), 1233 (s), 1210 (s), 1100 (w), 1045 (m), 1033 (m), 975 (w), 930 (m), 910 (w), 793 (m), 777 (m), 765 (m), 750 (m), 705 (m), 687 (m), 670 (m), 660 (m), 625 (w) cm⁻¹ ; ¹ H NMR (500 MHZ, CDCl₃) d 6.60 (dddd, J=16.8, 8.4, 8.4, 0.8 Hz, 1 H), 6.02 (apparent t, J=11.1 Hz, 1 H), 5.51 (dd, J=11.2, 7.9 Hz, 1 H), 5.42 (ddd, J=10.6, 10.6, 0.6 Hz, 1 H), 5.34 (apparent t, J=10.4 Hz, 1 H), 5.20 (dd, J=16.9, 1.9 Hz, 1 H), 5.16 (d, J=10.0 Hz, 1 H), 5.11 (d, J=10.1 Hz, 1 H), 4.77-4.69 (m, 1 H), 4.70 (dd, J=7.3, 4.2 Hz, 1 H), 4.60 (ddd, J=10.0, 10.0, 2.4 Hz, 1 H), 4.56 (br s, 2 H), 3.73 (m, 1 H), 3.28 (m, 1 H), 3.18 (dd, J=6.8, 4.8 Hz, 1 H), 2.98 (ddq, J=10.1, 6.9, 6.9 Hz, 1 H), 2.78 (ddq, J=9.8, 6.8, 6.8 Hz, 1 H), 2.66 (qd, J=7.3, 4.6 Hz, 1 H), 2.60-2.55 (m, 1 H), 2.10-1.80 (m, 10 H), 1.69 (ddd, J=14.4, 10.3, 3.1 Hz, 1 H), 1.64 (d, J=1.3 Hz, 3 H), 1.30 (d, J=7.4 Hz, 3 H), 1.06 (d, J=6.9 Hz, 3 H), 1.00 (d, J=6.8 Hz, 3 H), 0.99 (d, J=6.7 Hz, 3 H), 0.97 (d, J=6.8 Hz, 3 H), 0.94 (d, J=6.8 Hz, 3 H), 0.82 (d, J=6.3 Hz, 3 H); ¹³ C NMR (125 MHZ, CDCl₃) d 173.6, 157.0, 134.4, 133.7, 133.4, 132.9, 132.2, 129.9, 129.8, 117.9, 79.1, 78.9, 77.1, 75.7, 73.2, 64.4, 43.1, 41.0, 37.4, 36.1, 36.0, 35.8, 35.3, 34.8, 33.1, 23.3, 18.4, 17.4, 15.6, 15.5, 13.7, 12.5, 9.0; high resolution mass spectrum (FAB, NBA) m/z 616.3840 [(M+Na)⁺ ; calcd for C₃₃ H₅₅ NO₈ Na: 616.3826].

EXAMPLE 75 I. General Procedure for Synthesis of Siloxy Aldehydes (85)

A. A solution of organolithium (M=Li, FIG. 41))of type 80-83 (20 mmol) in ether (40 mL) is added slowly to a 0° C. solution of benzyl (S)-(+)-glycidyl ether (9 mmol) in ether (20 mL). The reaction is allowed to warm to room temperature. After 18-24 h, the reaction mixture is quenched by the addition of tert-butyldimethylsilyl triflate (10 mmol) and poured into saturated aqueous sodium bicarbonate (100 mL). The aqueous layer is separated and extracted with ether (2×50 mL). The combined organics are washed with saturated aqueous brine (50 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford an alpha-siloxy benzyl ether.

B. To a solution of the above benzyl ether (6 mmol) in ethyl acetate-ethanol (8:1, 90 mL) is added palladium on carbon (10% wet, 500 mg). The mixture is stirred under hydrogen atmosphere for 3-6 h, then filtered and concentrated in vacuo. The residue is purified by flash chromatography to afford an alcohol.

C. Aldehyde 85

Oxalyl chloride (1.5 mmol) is added dropwise to a -78° C. solution of dimethyl sulfoxide (3 mmol) in dichloromethane (4 mL). After 15 min, a -78° C. solution of the alcohol prepared in part B (1 mmol) in dichloromethane (2 mL) is added via canula. After an additional 15 min, diisopropylethylamine (4.5 mmol) is added and the reaction is gradually warmed to room temperature over 1 h and quenched with aqueous sodium bisulfate. The mixture is diluted with ether (50 mL) and is washed with water (2×30 mL), saturated aqueous brine (2×30 mL), is dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 85.

II. General Procedure for the Conversion of (85) to tetraene (86)

D. Phosphonium salt 75 (0.2 mmol) is dissolved in anhydrous tetrahydrofuran (2 mL) and chilled to 0° C. A solution of potassium bis(trimethylsilyl)amide (0.2 mmol, 0.5 20 M in tetrahydrofuran) is added and the reaction mixture is stirred 30 min at 0° C. After cooling to -78° C., a solution of aldehyde 85 (0.1 mmol) in tetrahydrofuran (2 mL) is added and the mixture is stirred 10 min at -78° C. and 2 h at room temperature. Saturated aqueous ammonium chloride (2 mL) is 25 added and the resultant mixture is extracted with ether (3×20 mL). The ethereal layer is washed with water (2×25 mL) and saturated aqueous brine (25 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford a tetraene.

E. To a solution of the tetraene prepared in part D (0.050 mmol) in dichloromethane (3 mL) at 0° C. is added water (0.050 mL) and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (0.018 mmol). After 1 h, the reaction mixture is diluted with ethyl acetate (50 mL), washed with saturated aqueous brine (3×25mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford an alcohol.

F. To a solution of the alcohol prepared in part E (0.010 mmol) in dichloromethane (2 mL) is added trichloroacetyl isocyanate (1.00 mmol). After 30 min, the reaction mixture is diluted with dichloromethane (4 mL) and neutral alumina (1 g) is added. The resultant suspension is stirred an additional 4 h. The reaction mixture is filtered and the concentrated filtrate is chromatographed on silica gel to afford a carbamate.

G. Analog 86

A solution of the carbamate prepared in part F (0.010 mmol) in 48% hydrofluoric acid-acetonitrile (1:9, 2 mL) is stirred at ambient temperature. After 12 h, saturated aqueous sodium bicarbonate (25 mL) is added and the mixture is extracted with ethyl acetate (3×20 mL). The combined organics are dried over magnesium sulfate and concentrated in vacuo. The residue is purified by flash chromatography to afford 86.

Those skilled in the art will appreciate that numerous changes and modifications may be made to the preferred embodiments of the invention and that such changes and modifications may be made without departing from the spirit of the invention. It is therefore intended that the appended claims cover all equivalent variations as fall within the true spirit and scope of the invention. 

What is claimed is:
 1. A process for producing a diene having formula: ##STR71## wherein: R₁, R₂, R₇, R₈, R₁₁, and R₁₂ are, independently, C₁ -C₁₀ alkyl;R₃, R₆ and R₁₆ are, independently, selected from the group consisting of hydrogen and C₁ -C₆ alkyl; R₄, R₉, R₁₄ and R₁₅ are, independently, acid labile hydroxyl protecting groups; and R₂₅ is an acid stable hydroxyl protecting group; comprising contacting a phosphonium salt having formula: ##STR72## wherein R₁₈ is C₁ -C₆ aryl and X is a halogen with a base and a compound having formula: ##STR73## for a time and under conditions effective to form said diene.
 2. The process according to claim 1, wherein:R₁, R₂, R₃, R₆, R₇, R₈, R₁₁, and R₁₂ are methyl; R₄, R₉, R₁₄, and R₁₅ are t-butyldimethysilyl; and R₂₅ is p-methoxybenzyl.
 3. A compound having one of the following formulas: ##STR74## wherein: Z₁ and Z₂ are O;R₁, R₂, R₇, R₈, R₁₁, and R₁₂ are, independently, C₁ -C₁₀ alkyl; R₃ and R₆ are, independently, selected from the group consisting of hydrogen and C₁ -C₆ alkyl; R₄, R₉, R₁₄ and R₁₅ are, independently, acid labile hydroxyl protecting groups; R₅ is C₆ to C₁₄ aryl; R₂₅ is an acid stable hydroxyl protecting group; and R₁₆ is selected from the group consisting of hydrogen and C₁ -C₆ alkyl; H or C₁ -C₆ alkyl. 